[go: up one dir, main page]

WO2009062905A1 - Pesticidal mixtures comprising cyanosulfoximine compounds - Google Patents

Pesticidal mixtures comprising cyanosulfoximine compounds Download PDF

Info

Publication number
WO2009062905A1
WO2009062905A1 PCT/EP2008/065213 EP2008065213W WO2009062905A1 WO 2009062905 A1 WO2009062905 A1 WO 2009062905A1 EP 2008065213 W EP2008065213 W EP 2008065213W WO 2009062905 A1 WO2009062905 A1 WO 2009062905A1
Authority
WO
WIPO (PCT)
Prior art keywords
methyl
carboxamide
pyrazole
difluoromethyl
active compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2008/065213
Other languages
French (fr)
Inventor
Delphine Breuninger
Henricus Maria Martinus Bastiaans
Wolfgang Von Deyn
Matthias Pohlman
Jürgen LANGEWALD
Egon Haden
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BR122018004457-8A priority Critical patent/BR122018004457B1/en
Priority to CN200880124587XA priority patent/CN101909448A/en
Priority to BRPI0819823A priority patent/BRPI0819823B1/en
Priority to BR122018016271-6A priority patent/BR122018016271B1/en
Priority to ES08851006.0T priority patent/ES2554768T3/en
Priority to US12/742,766 priority patent/US20110105321A1/en
Priority to JP2010533550A priority patent/JP2011503138A/en
Priority to PL08851006T priority patent/PL2219456T3/en
Application filed by BASF SE filed Critical BASF SE
Priority to EP08851006.0A priority patent/EP2219456B1/en
Publication of WO2009062905A1 publication Critical patent/WO2009062905A1/en
Priority to IL205622A priority patent/IL205622A0/en
Anticipated expiration legal-status Critical
Priority to US14/136,863 priority patent/US20140179518A1/en
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
    • A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16—Heavy metals; Compounds thereof
    • A01N59/20—Copper

Definitions

  • Pesticidal mixtures comprising cyanosulfoximine compounds
  • the present invention relates to mixtures of active ingredients having synergistically enhanced action and to methods comprising applying said mixtures.
  • Another problem encountered concerns the need to have available pest control agents which are effective against a broad spectrum of pests.
  • compositions that improve plants a process which is commonly and hereinafter referred to as "plant health".
  • plant health a process which is commonly and hereinafter referred to as "plant health".
  • advantageous properties are improved crop characteristics including: emergence, crop yields, protein content, more developed root system, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less fertilizers needed, less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, enhanced plant vigor, increased plant stand and early germination; or any other advantages familiar to a person skilled in the art.
  • Methods for improving the health of plants by applying active compounds to the plants or the locus are a general need.
  • Another difficulty in relation to the use of pesticides is that the repeated and exclusive application of an individual pesticidal compound leads in many cases to a rapid selection of pests which have developed natural or adapted resistance against the active compound in question.
  • the present invention relates to pesticidal mixtures comprising, as active compounds,
  • active compound I at least one insecticidal compound of formula
  • R 1 is Cl or CF 3
  • R 2 is selected from hydrogen, chloro, CH 3 or C 2 H 5 ;
  • a azoles such as triazoles, imidazoles, pyrazoles, thiazoles and oxazoles selected from the group consisting of azaconazole, benomyl, bitertanol, bromuconazole, carbendazim, cyproconazole, cyazofamid, difenoconazole, diniconazole, diniconazole-M, enilconazole, epoxiconazole, ethaboxam, etridiazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, fuberidazole, hexaconazole, hymexazole, imazalil, imazalil-sulfphate, imibenconazole, ipconazole, metconazole, myclobutanil,
  • B strobilurins selected from the group consisting of azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyribencarb, trifloxystrobin, methyl 2-(ortho-(2,5- dimethylphenyloxymethylene)phenyl)-3-methoxy-acrylate, 2-(2-(6-(3- chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2- methoxyimino-N-methyl-acetamide and 3-methoxy-2-(2-(N-(4- methoxy-phenyO-cyclo-propanecarboximidoylsulfanylmethyO-phenyl)- acrylic acid methyl ester;
  • C carboxamides selected from the group consisting of benalaxyl, benalaxyl-M, benodanil, bixafen, boscalid, carboxin, carpropamid, dimethomorph, diclocymet, fenhexamid, fluopyram, flutolanil, furametpyr, flumorph, flumetover, fluopicolide (picobenzamid), isopyrazam, mandipropamid, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, oxytetracyclin, penthiopyrad, silthiofam,thifluzamide, tiadinil, zoxamide, 5-fluoro-1 ,3-dimethyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,2-dimethyl- propyl)-phenyl]-amide, methyl-3-(4-chlor
  • heterocyclic compounds selected from the group consisting of acibenzolar-S-methyl, anilazine, aldimorph, blasticidin-S, bupirimate, captafol, captan, chinomethionat, cyprodinil, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulphat, diflumetorim, dodemorph, dodemorph-acetate, famoxadone, fenamidone, fenarimol, ferimzone, fenpiclonil, fenpropidin, fenpropimorph, fludioxonil, fluazinam, fluoroimid, flutianil, folpet, fenoxanil, iprodione, mepanipyrim, nitrapyrin, nuarimol, octhilinone, oxolinic acid, piperalin, probenazole, procy
  • [1 ,2,4]triazolo[1 ,5-a]py ⁇ imidine-7-ylamine 5-methyl-6-(3,5,5-trimethyl- hexyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-ylamine, 5-methyl-6-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 6-methyl-5-octyl- [1 ,2,4]tri-azolo[1 ,5-a]pyrimidine-7-yl-amine, 6-ethyl-5-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 5-ethyl-6-octyl-
  • carbamates selected from the group consisting of diethofencarb, ferbam, flubenthiavalicarb, iprovalicarb, mancozeb, maneb, metam, methasulphocarb, metiram, propamocarb, propamocarb hydrochlorid,propineb, thiram, zineb, ziram, 4-fluorophenyl N-(1-(1-(4- cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, methyl 3-(4- chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate and carbamate oxime ethers of the formula
  • various fungicides selected from the group of antibiotics comprising kasugamycin, kasugamycin-hydrochlorid-hydrat , mildiomycin, streptomycin, polyoxin and validamycin A; the group of nitrophenyl derivatives comprising binapacryl, dinocap, dinobuton, dicloran, nitrothal-isopropyl and tecnazen; the group of sulfur-containing heterocyclyl compounds comprising dithianon and isoprothiolane; the group of organometallic compounds comprising fentin salts; the group oforganophosphorus compounds comprising edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos and tolclofos-methyl; the group of organochlorine compounds comprising chlorothalonil, dichlofluanid, dichlorophen, pentachlorophenol and its salts, flusulfamide,
  • active compounds I of the formula I their preparation and their action against insect and acarid pests have been described in WO 2006/060029 and in WO 2007/095229. Preparation methods of active compounds I of formula I can be found therein.
  • Benalaxyl methyl N-(phenylacetyl)-N-(2,6-xylyl)-DL-alaninate (DE 29 03 612); metalaxyl, methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate (GB 15 00 581 ); ofurace, (RS)- ⁇ -(2-chloro-N-2,6-xylylacetamido)- ⁇ -butyrolactone [CAS RN 58810-48-
  • aldimorph " 4-alkyl-2,5(or 2,6)-dimethylmorpholine” , comprising 65-75% of 2,6- dimethylmorpholine and 25-35% of 2,5-dimethylmorpholine, comprising more than 85% of 4-dodecyl-2,5(or 2,6)-dimethylmorpholine, where " a l kyl” also includes octyl, decyl, tetradecyl and hexadecyl, with a cis/trans ratio of 1 :1 [CAS RN 91315-15-0]; dodine, 1-dodecylguanidinium acetate (Plant Dis. Rep., Vol.
  • streptomycin 1 ,1 '- ⁇ 1-L-(1 ,3,5/2,4,6)-4-[5-deoxy-2-O-(2-deoxy-2-methylamino- ⁇ -L- glucopyranosyl)-3-C-formyl- ⁇ -L-lyxofuranosyloxy]-2,5,6-trihydroxycyclohex-1 ,3- ylene ⁇ diguanidine (J. Am. Chem. Soc. Vol.
  • bitertanol ⁇ -([1 ,1'-biphenyl]-4-yloxy)- ⁇ -(1 ,1-dimethylethyl)-1 H-1 ,2,4-triazole-1-ethanol
  • prothioconazole 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4- dihydro[1 ,2,4]triazole-3-thione (WO 96/16048); simeconazole, ⁇ -(4-fluorophenyl)- ⁇ -[(trimethylsilyl)methyl]-1 H-1 ,2,4-triazole-1-ethanol [CAS RN 149508-90-7], tebuconazole, 1 -(4-chlorophenyl)-4,4-dimethyl-3-[1 ,2,4]triazol-1 -ylmethylpentan-3-ol (EP-A 40 345); tetraconazole, 1-[2-(2,4-dichlorophenyl)-3-(1 ,1 ,2,2-tetrafluoroethoxy)propyl]-1 H-1 ,2,4- triazole (WO 96/16048
  • fuberidazole 2-(2-furanyl)-1 H-benzimidazole (DE-A 12 09 799); flutolanil, ⁇ , ⁇ , ⁇ -trifluoro-3'-isopropoxy-o-toluanilide (JP 1104514); furametpyr, 5-chloro-N-(1 ,3-dihydro-1 ,1 ,3-trimethyl-4-isobenzofuranyl)-1 ,3-dimethyl-1 H- py ⁇ azole-4-carboxamide [CAS RN 123572-88-3]; isoprothiolane, diisopropyl 1 ,3-dithiolan-2-ylidenemalonate (Proc. Insectic. Fungic.
  • flubenthiavalicarb (benthiavalicarb), isopropyl ⁇ (S)-1-[(1 R)-1-(6-fluorobenzothiazol-2-yl)- ethylcarbamoyl]-2-methylpropyl ⁇ carbamate (JP-A 09/323 984); carpropamid, 2,2-dichloro-N-[1 -(4-chlorophenyl)ethyl]-1 -ethyl-3-methylcyclopropane- carboxamide [CAS RN 104030-54-8]; chlorothalonil, 2,4,5,6-tetrachloroisophthalonitrile (US 3 290 353); cyflufenamid, (Z)-N-[ ⁇ -(cyclopropylmethoxyimino)-2,3-difluoro-6-
  • N-(2-Bicycloprop-2-ylphenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide is a mixture of the diastereomers N-(trans-2-bicycloprop-2-ylphenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide and N-(cis-2-bicycloprop-2-ylphenyl)-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide (WO 03/074491 and WO
  • the present invention relates to: agricultural compositions comprising a mixture of at least one active compound I and at least one active compound II; - the use of a mixture of at least one active compound I and at least one active compound Il for combating animal pests; the use of a mixture of at least one active compound I and at least one active compound Il for combating phytopathogenic harmful fungi; a method of combating animal pests which comprises contacting the animal pests, their habit, breeding ground, food supply, plant, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal attack or infestation with a pesticidally effective amount of a mixture of at least one active compound I and at least one active compound II; a method for protecting crops from attack or infestation by animal pests and/or phythopathogenic harmful fungi, which comprises contacting a crop with a mixture of at least one active compound I and at least one active compound II; a method for the protection of seeds
  • the compounds I can be used as synergists for a large number of different fungicidal active compounds.
  • simultaneous, that is joint or separate, application of compound(s) I with at least one active compound II the fungicidal and/or insecticidal activity is increased in a superadditive manner.
  • the compounds I can be present in different crystal modifications, which may differ in biological activity.
  • active compounds I of formula I are preferred, wherein
  • R 1 is CF 3
  • active compounds I of formula I are preferred, wherein
  • R 1 is Cl
  • active compounds I of formula I are preferred, wherein G is G 1 and
  • active compounds I of formula I are also preferred, wherein
  • G is G 1 and
  • R 2 is hydrogen, chloro, or C2H5;
  • active compounds I of formula I are also preferred, wherein
  • G is G 2 and
  • R 2 is hydrogen
  • the compounds of formula I include racemic mixtures, individual pure enantiomers and diasteroemers and optically active mixtures.
  • active compound Il selected from the group II.A of azoles consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, propiconazole, prothioconazole, triadimef
  • active compound Il selected from the group II.A of azoles consisting of benomyl, carbendazim, , epoxiconazole, fluquinconazole, flutriafol, flusilazole, metconazole, prochloraz, prothioconazole, tebuconazole and triticonazole.
  • B of strobilurins consisting of azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin and trifloxystrobin.
  • B of strobilurins consisting of azoxystrobin, kresoxim-methyl, orysastrobin and pyraclostrobin.
  • C of carboxamides consisting of bixafen, boscalid, carpropamid, dimethomorph, fenhexamid, flumorph, fluopicolide (picobenzamid), fluopyram, isothianil, mandipropamid, metalaxyl, mefenoxam, ofurace, penthiopyrad and zoxamide.
  • C of carboxamides consisting of boscalid, carpropamid, dimethomorph, fenhexamid, fluopicolide, fluopyram, mandipropamid, metalaxyl, mefenoxam, ofurace, penthiopyrad and zoxamide.
  • C of carboxamides consisting of boscalid, dimethomorph and penthiopyrad.
  • D of heterocyclic compounds consisting of acibenzolar-S-methyl, captafol, cyprodinil, dodemorph, famoxadone fenamidone, fenarimol, fenpropimorph, fenpropidin, fenoxanil, fludioxonil, fluazinam, folpet, iprodione, mepanipyrim, probenazole, proquinazid, pyrimethanil, quinoxyfen triforine, tridemorph, vinclozolin and 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)- [1 ,2,4]triazolo[1 ,5-a]pyrimidine.
  • D of heterocyclic compounds consisting of dodemorph, famoxadone, fenpropimorph, iprodione, proquinazid , pyrimethanil, quinoxyfen, tridemorph, vinclozolin and 5-chloro-7-(4-methylpiperidin-1- yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine.
  • D of heterocyclic compounds consisting of dodemorph, famoxadone, fenpropimorph, proquinazid pyrimethanil, tridemorph and 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6- trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine.
  • E of carbamates consisting of iprovalicarb, flubenthiavalicarb, maneb, mancozeb, metiram, propineb, propamocarb and thiram.
  • E of carbamates consisting of iprovalicarb, flubenthiavalicarb, maneb, mancozeb, metiram and thiram.
  • mixtures mixtures of a compound of the formula I with at least one active compound Il selected from the group II are particularly preferred.
  • F of other fungicides consisting of chlorothalonil, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, cymoxanil, dichlofluanid, dithianon, fentin salts, such as fentin acetate, fosetyl, fosetyl-aluminum, flusulfamide, metrafenone, phosphorous acid and its salts, thiophanate-methyl, sulfur and spiroxamine.
  • mixtures of a compound of the formula I with at least one active compound Il selected from the group II F of other fungicides consisting of chlorothalonil, dithianon, flusulfamide, fosetyl-aluminium, metrafenone, phosphorous acid and its salts and thiophanate-methyl.
  • F of other fungicides consisting of chlorothalonil, dithianon, flusulfamide, metrafenone and phosphorous acid and its salts.
  • the mixtures of the present invention have excellent activity against a broad spectrum of phytopathogenic fungi and animal pests.
  • Animal pests The mixtures of the present invention have excellent activity against a broad spectrum of animal pests.
  • arthropodal pests such as arachnids, myriapedes and insects as well as nematodes.
  • insects are suitable for controlling insect pests, such as insects from the order of
  • lepidopterans for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis viresc
  • beetles Coldeoptera
  • Agrilus sinuatus for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Aphthona euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Ctenicera ssp., Diabrotica longi
  • mosquitoes e.g. Aedes aegypti, Aedes albopictus, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Contarinia sorghicola Cordylobia anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus
  • thrips (Thysanoptera), e.g. Dichromothrips corbetti, Dichromothrips ssp., Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci,
  • Isoptera e.g. Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Reticulitermes santonensis, Reticulitermes grassei, Termes natalensis, and Coptotermes formosanus;
  • cockroaches e.g. Blattella germanica, Blattella asahinae, Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis;
  • insects e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus,
  • crickets grasshoppers, locusts (Orthoptera), e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Hieroglyphus daganensis, Kraussaria angulifera, Calliptamus italicus, Chortoicetes terminifera, and Locustana pardalina;
  • Orthoptera e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria
  • arachnoidea such as arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and
  • Sarcoptidae such as Amblyomma americanum, Amblyomma variegatum, Ambryomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor andersoni, Dermacentor variabilis, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi, Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes
  • Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and Oligonychus pratensis; Araneida, e.g. Latrodectus mactans, and Loxosceles reclusa;
  • fleas e.g. Ctenocephalides felis, Ctenocephalides canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus,
  • silverfish, firebrat e.g. Lepisma saccharina and Thermobia domestica
  • centipedes Chilopoda
  • Scutigera coleoptrata centipedes
  • Earwigs e.g. forficula auricularia
  • Pediculus humanus capitis e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus.
  • Collembola (springtails), e.g. Onychiurus ssp..
  • Nematodes plant parasitic nematodes such as root knot nematodes, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, and other Meloidogyne species; cyst-forming nematodes, Globodera rostochiensis and other Globodera species; Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, and other Heterodera species; Seed gall nematodes, Anguina species; Stem and foliar nematodes, Aphelenchoides species; Sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; Pine nematodes, Bursaphelenchus xylophilus and other Bursaphelenchus species; Ring nematodes, Criconema
  • arachnids such as acarians (Acarina), e.g. of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp.
  • arachnoidea such as acarians (Acarina)
  • Tetranychidae spp. such as Aculus Basilendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp. such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp. such as Brevipalpus phoenicis; Tetranychidae spp. such as
  • Tetranychus cinnabarinus Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and oligonychus pratensis.
  • the mixtures of the present invention have excellent activity against a broad spectrum of phytopathogenic fungi Ascomycetes, Basidiomycetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). Some of them are systemically effective and can be employed in crop protection as foliar fungicides, as fungicides for seed dressing and as soil fungicides. They can also be used for treating seed.
  • Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and grapevines;
  • Cochliobolus species on corn, cereals, rice for example Cochliobolus sativus on cereals, Cochliobolus miyabeanus on rice;
  • Drechslera species Pyrenophora species on corn, cereals, rice and lawns, for example, D. teres on barley or D. tritici-repentis on wheat;
  • Fusarium and Verticillium species on various plants for example, F graminearum or F. culmorum on cereals or F. oxysporum on a multitude of plants, such as, for example, tomatoes;
  • Gibberella species on cereals and rice for example Gibberella fujikuroi on rice
  • Mycosphaerella species on cereals, bananas and peanuts for example, M. graminicola on wheat or M.fijiensis on bananas;
  • Peronospora species on cabbage and bulbous plants for example, P. brassicae on cabbage or P. destructor on onions; - Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans;
  • Phytophthora species on various plants for example, P. capsici on bell pepper;
  • Pseudocercosporella herpotrichoides on cereals Pseudoperonospora on various plants, for example, P. cubensis on cucumber or
  • Puccinia species on various plants for example, P. triticina, P. striformins, P. hordei or P.graminis on cereals or P. asparagi on asparagus; - Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S.attenuatum,
  • Rhynchosporium secalis on barley, rye and triticale Rhynchosporium secalis on barley, rye and triticale; - Sclerotinia species on oilseed rape and sunflowers;
  • Ustilago species on cereals, corn and sugar cane for example, U. maydis on corn;
  • the mixtures according to the invention are also suitable for controlling harmful fungi in the protection of materials (for example wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products.
  • harmful fungi Ascomycetes, such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes, such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp.
  • Tyromyces spp. Deuteromycetes, such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes, such as Mucor spp., additionally in the protection of materials the following yeasts: Candida spp. and Saccharomyces cerevisae.
  • the pesticidal mixtures according to the present invention can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compounds according to the invention.
  • auxiliaries suitable for the formulation of agrochemicals such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, antifoaming agents, anti-freezing agents, for seed treatment formulation also optionally gelling agents.
  • solvents examples include water, aromatic solvents (for example SolvessoTM products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP(N-methyl-pyrrolidone), NOP (N-octyl- pyrrolidone)), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used.
  • aromatic solvents for example SolvessoTM products, xylene
  • paraffins for example mineral oil fractions
  • alcohols for example methanol, butanol, pentanol, benzyl alcohol
  • ketones for example cyclohexanone, gamma-butyrolactone
  • Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates).
  • dispersants examples include lignin-sulfite waste liquors and methylcellulose.
  • Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalene- sulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl
  • Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
  • mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin
  • anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.
  • Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate.
  • a suitable preservative is e.g. dichlorophen.
  • gelling agent is carrageen (Satiagel®)
  • Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
  • Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
  • solid carriers examples include mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
  • mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate
  • the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compounds.
  • the active compounds are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight (according to NMR spectrum or HLPC spectrum).
  • respective formulations can be diluted 2-10 fold leading to concentrations in the ready to use preparations of 0,01 to 60% by weight active compounds by weight, preferably 0,1 to 40% by weight.
  • mixtures of the present invention can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring.
  • the use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention.
  • Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier.
  • concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil and such concentrates are suitable for dilution with water.
  • the active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 % per weight.
  • the active compound(s) may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
  • UUV ultra-low-volume process
  • Products for dilution with water for foliar applications may be applied to the seed diluted or undiluted.
  • the active compound(s) 10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound(s) dissolve(s) upon dilution with water, whereby a formulation with 10 % (w/w) of active compound(s) is obtained.
  • DC Dispersible concentrates 20 parts by weight of the active compound(s) are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compound(s) is obtained.
  • a dispersant for example polyvinylpyrrolidone
  • Emulsions EW, EO, ES
  • 25 parts by weight of the active compound(s) are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is introduced into 30 parts by weight of water by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound(s) is obtained.
  • an emulsifier machine e.g. Ultraturrax
  • 50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluid- ized bed). Dilution with water gives a stable dispersion or solution of the active compound ⁇ ), whereby a formulation with 50% (w/w) of active compound(s) is obtained.
  • Products to be applied undiluted for foliar applications may be applied to the seed diluted or undiluted.
  • 0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound ⁇ ) is obtained.
  • Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.
  • oils, wetters, adjuvants or bactericides may be added to the active ingredients.
  • Suitable adjuvants in this context are, in particular: organically modified polysiloxanes, e.g. Break Thru S 240TM; alcohol alkoxylates, e.g. Atplus 245TM, Atplus MBA 1303TM, Plurafac LF 300TM and Lutensol ON 30TM; EO/PO block polymers, e.g. Pluronic RPE 2035TM and Genapol BTM; alcohol ethoxylates, e.g. Lutensol XP 80TM; and sodium dioctylsulfosuccinate, e.g. Leophen RATM.
  • Compositions of this invention may further contain other active ingredients than those listed above.
  • active ingredients for example further insecticides or fungicides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators and safeners.
  • These agents usually are admixed with the agents according to the invention in a weight ratio of 1 :10 to 10:1.
  • the pesticidal mixtures may comprise additionally one or more further insecticidal compound III of the following list M of pesticides.
  • the list is intended to illustrate the possible combinations, but not to impose any limitation:
  • Organo(thio)phosphates acephate, azamethiphos, azinphos-ethyl, azinphos- methyl, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos- methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/ DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, flupyrazophos, fosthiazate, heptenophos, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl
  • Nicotinic receptor agonists/antagonists compounds acetamiprid, bensultap, cartap hydrochloride, clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, nicotine, spinosad (allosteric agonist), thiacloprid, thiocyclam, thiosultap- sodium and AKD1022.
  • GABA gated chloride channel antagonist compounds chlordane, endosulfan, gamma-HCH (lindane); acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole, the phenylpyrazole compound of formula M 6 1
  • Chloride channel activators abamectin, emamectin benzoate, milbemectin, lepimectin;
  • METI I compounds fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad, flufenerim, rotenone;
  • METI Il and III compounds acequinocyl, fluacyprim, hydramethylnon;
  • M.1 Inhibitors of oxidative phosphorylation: azocyclotin, cyhexatin, diafenthiuron, fenbutatin oxide, propargite, tetradifon;
  • Moulting disruptors cyromazine, chromafenozide, halofenozide, methoxyfenozide, tebufenozide;
  • Lipid biosynthesis inhibitors spirodiclofen, spiromesifen, spirotetramat
  • ryanodine receptor modulators flubendiamide
  • R M " 22 is methyl or ethyl and Het * is 3,3-dimethylpyrrolidin-1-yl, 3- methylpiperidin-1 -yl, 3,5-dimethylpiperidin-1 -yl, 3-trifluormethylpiperidin-1 -yl, hexahydroazepin-1-yl, 2,6-dimethylhexahydroazepin-1-yl or 2,6-dimethylmorpholin-4-yl.
  • CF 3 CF 2 CH 2 C(CN) 2 CH 2 (CF 2 )SCF 2 H, 2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,4,4,4- pentafluorobutyl)-malonodinitrile, and CF 2 HCF 2 CF 2 CF 2 CH 2 C(CN) 2 CH 2 CH 2 CF 2 CF 3 ;
  • Anthranilamide derivatives of formula M 24 1 have been described in WO 01/70671 , WO 04/067528 and WO 05/1 18552. Cyflumetofen and its preparation have been described in WO 04/080180. The aminoquinazolinone compound pyrifluquinazon has been described in EP A 109 7932. The alkynylether compounds M 22 1 and M 222 are described e.g. in JP 2006131529.
  • the malononitrile compounds CF 3 (CH 2 ) 2 C(CN) 2 CH 2 (CF 2 ) 3 CF 2 H, CF 3 (CH 2 ) 2 C(CN) 2 CH 2 (CF 2 ) 5 CF 2 H, CF 3 (CH 2 ) 2 C(CN) 2 (CH 2 ) 2 C(CF 3 ) 2 F, CF 3 (CH 2 ) 2 C(CN) 2 (CH 2 ) 2 (CF 2 ) 3 CF 3 , CF 2 H(CF 2 ) 3 CH 2 C(CN) 2 CH 2 (CF 2 ) 3 CF 2 H, CF 3 (CH 2 ) 2 C(CN) 2 CH 2 (CF 2 ) 3 CF 3 , CF 3 (CF 2 ) 2 CH 2 C(CN) 2 CH 2 (CF 2 ) 3 CF 2 H, CF 3 CF 2 CH 2 C(CN) 2 CH 2 (CF 2 )SCF 2 H, 2- (2,2,3,3,4,4,5,5-octafluoropentyl)
  • compositions of this invention may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix).
  • the plant(s) may be sprayed with a composition of this invention either before or after being treated with other active ingredients.
  • the one or more active compound(s) I and the one or more active compound(s) Il can be applied according to different ways of applications, which are I. simultaneously, that is a) jointly (i.e. as mixture as such, e.g. a ready-to-use-formulation, or as tank mix) or b) separately (i.e. application via separate tanks), or
  • the method for controlling harmful fungi and animal pests is carried out by the separate or joint application of at least one active compound I and at least one of the active compound II, or a mixture of at least one active compounds I and at least one of the active compound II, by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
  • inventive mixtures or compositions of these mixtures can also be employed for protecting plants from attack or infestation by insects, acarids or nematodes comprising contacting a plant, or soil or water in which the plant is growing.
  • the term plant refers to an entire plant, a part of the plant or the propagation material of the plant, that is, the seed or the seedling.
  • Plants which can be treated with the inventive mixtures include all genetically modified plants or transgenic plants, e.g. crops which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods, or plants which have modified characteristics in comparison with existing plants, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures.
  • Some of the inventive mixtures have systemic action and can therefore be used for the protection of the plant shoot against foliar pests as well as for the treatment of the seed and roots against soil pests.
  • the mixtures of compounds I and Il or their corresponding formulations are applied by treating the harmful fungi and the animal pests, their habitat or the plants, seeds, soils, areas, materials or spaces to be kept free from them with a pesticidally effective amount of the mixture or, in the case of separate application, of the compounds I and II.
  • Application can be before or after the infection by harmful fungi and/or animal pests.
  • pesticidally effective amount means the amount of the inventive mixtures or of compositions comprising the mixtures needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism.
  • the pesticidally effective amount can vary for the various mixtures / compositions used in the invention.
  • a pesticidally effective amount of the mixtures / compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.
  • Preferred application methods are into water bodies, via soil, cracks and crevices, pastures, manure piles, sewers, into water, on floor, wall, or by perimeter spray application and bait.
  • mixtures of at least one compound I and at least one active compound Il are employed.
  • mixtures of at least one compound I with two or, if desired, more active components may also offer particular advantages.
  • Suitable further active components in the above sense are particularly the active compounds Il mentioned at the outset and in particular the preferred active compounds Il mentioned above.
  • inventive mixtures and the compositions comprising them can be used for protecting wooden materials such as trees, board fences, sleepers, etc. and buildings such as houses, outhouses, factories, but also construction materials, furniture, leathers, fibers, vinyl articles, electric wires and cables etc. from ants and/or termites, and for controlling ants and termites from doing harm to crops or human being (e.g. when the pests invade into houses and public facilities).
  • the quantity of active ingredient(s) ranges from 0.0001 to 500 g per 100 m 2 , preferably from 0.001 to 2O g per 100 m 2 .
  • Customary application rates in the protection of materials are, for example, from 0.01 g to 1000 g of active compound(s) per m 2 treated material, desirably from 0.1 g to 50 g per m 2 .
  • Pesticidal compositions for use in the impregnation of materials typically contain from 0.001 to 95 weight %, preferably from 0.1 to 45 weight %, and more preferably from 1 to 25 weight % of at least one repellent and / or insecticide.
  • the content of the mixture of the active ingredients is from 0.001 to 80 weights %, preferably from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight %.
  • “synergistically effective amount” means that the one or more active compound(s) I and the one or more active compound(s) Il are usually applied in a weight ratio of from 500:1 to 1 :100, preferably from 20:1 to 1 :50, in particular from 5:1 to 1 :20.
  • the employed weight ratio of compound(s) I and compound(s) Il ranges can start from 100:1 to 1 :100, preferably from 20:1 to 1 :20, in particular from 10:1 to 1 :10.
  • the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 20 to 1500 g/ha, more preferably from 50 to 1000 g/ha and in particular from 50 to 750 g/ha.
  • the rate of application of the mixture of the active ingredients of this invention may be in the range of 0.1 g to 4000 g per hectare, desirably from 25 g to 600 g per hectare, more desirably from 50 g to 500 g per hectare.
  • the application rates for the compound(s) I are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
  • the application rates for the active compound Il are generally from 1 to 2000 g/ha, preferably from 10 to 1500 g/ha, in particular from 40 to 1000 g/ha.
  • Methods to control infectious diseases transmitted by insects with the inventive mixtures and their respective compositions also comprise treating surfaces of huts and houses, air spraying and impregnation of curtains, tents, clothing items, bed nets, tsetse-fly trap or the like, lnsecticidal compositions for application to fibers, fabric, knitgoods, non- wovens, netting material or foils and tarpaulins preferably comprise a composition including the inventive mixtures, optionally a repellent and at least one binder.
  • Bait formulations and applications The mixtures according to the invention can be applied to any and all developmental stages, such as egg, larva, pupa, and adult.
  • the pests may be controlled by contacting the target pest, its food supply, habitat, breeding ground or its locus with a pesticidally effective amount of the inventive mixtures or of compositions comprising the mixtures.
  • Locus in general means a plant, seed, soil, area, material or environment in which pests or fungi are growing or may grow.
  • the mixtures according to the invention are effective through both contact and ingestion.
  • the inventive mixtures are effective through both contact (via soil, glass, wall, bed net, carpet, plant parts or animal parts), and ingestion (bait, or plant part) and through trophallaxis and transfer.
  • the inventive mixtures are prepared into a bait preparation.
  • the bait can be a liquid, a solid or a semisolid preparation (e.g. a gel).
  • the bait employed in the composition is a product which is sufficiently attractive to incite insects such as ants, termites, wasps, flies, mosquitoes, crickets etc. or cockroaches to eat it.
  • This attractant may be chosen from feeding stimulants or para and / or sex pheromones readily known in the art.
  • the typical content of active ingredient(s) is from 0.0001 weight % to 15 weight %, desirably from 0.001 weight % to 5% weight % of active compound.
  • the composition used may also comprise other additives such as a solvent of the active material, a flavoring agent, a preserving agent, a dye or a bitter agent. Its attractiveness may also be enhanced by a special color, shape or texture.
  • the mixtures according to the present invention are employed via soil application.
  • Soil application is especially favorable for use against ants, termites, crickets, or cockroaches.
  • the mixtures according to the present invention are prepared into a bait preparation.
  • the mixtures according to the present invention are also suitable for the treatment of seeds in order to protect the seed from harmful fungi and animal pests, in particular from soil-living fungi and insect pests and the resulting plant's roots and shoots against soil pests and foliar insects.
  • the protection of the resulting plant's roots and shoots is preferred.
  • the present invention therefore comprises therefore a method for the protection of seeds from insects, in particular from soil pests and of the seedlings' roots and shoots from harmfulo fungi and insects, in particular from soil and foliar insects, said method comprising contacting the seeds before sowing and/or after pregermination with mixtures according to the present invention.
  • Particularly preferred is a method, wherein the plant's roots and shoots are protected.
  • seed embraces seeds and plant propagules of all kinds including but not limited to true seeds, seed pieces, suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots and the like and means in a preferred embodiment true seeds.
  • seed treatment comprises all suitable seed treatment techniques known in the art, such as seed dressing, seed coating, seed dusting, seed soaking and seed pelleting.
  • the present invention also comprises seeds coated with or containing the active compounds.
  • coated with and/or containing generally signifies that the active ingredients are for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product are (re)planted, it may absorb the active ingredient.
  • Suitable seeds are seeds of cereals, root crops, oil crops, vegetables, spices, ornamentals, for example seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geranium/pelargoniums, pansies and impatiens.
  • mixtures according to the invention may also be used for the treatment seeds from plants, which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods.
  • the active mixtures can be employed in treatment of seeds from plants, which are resistant to herbicides from the group consisting of the sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogous active substances (see for example, EP-A-0242236, EP-A-242246) (WO 92/00377) (EP-A-0257993, U.S. Pat. No. 5,013,659) or in transgenic crop plants, for example cotton, with the capability of producing Bacillus thuringiensis toxins (Bt toxins) which make the plants resistant to certain pests (EP-A-0142924, E P-A-0193259),
  • the mixtures according to the present invention can be used also for the treatment of seeds from plants, which have modified characteristics in comparison with existing plants consist, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures).
  • a number of cases have been described of recombinant modifications of crop plants for the purpose of modifying the starch synthesized in the plants (e.g. WO 92/11376, WO 92/14827, WO 91/19806) or of transgenic crop plants having a modified fatty acid composition (WO 91/13972).
  • the seed treatment application of the mixtures is carried out by spraying or by dusting the seeds before sowing of the plants and before emergence of the plants.
  • the corresponding formulations are applied by treating the seeds with an effective amount of the mixture according to the present invention.
  • the application rates of the active compound(s) are generally from 0,1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 2,5 kg per 100 kg of seed. For specific crops such as lettuce the rate can be higher.
  • compositions which are especially useful for seed treatment are e.g.:
  • a Soluble concentrates (SL, LS)
  • Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulations can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds or after having pregerminated the latter
  • a FS formulation is used for seed treatment.
  • a FS formulation may comprise 1-800 g/l of active ingredient(s), 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.
  • Preferred FS formulations of the active compounds for seed treatment usually comprise from 0.1 to 80% by weight (1 to 800 g/l) of the active ingredient(s), from 0.1 to 20 % by weight (1 to 200 g/l) of at least one surfactant, e.g. 0.05 to 5 % by weight of a wetter and from 0.5 to 15 % by weight of a dispersing agent, up to 20 % by weight, e.g. from 5 to 20 % of an anti-freeze agent, from 0 to 15 % by weight, e.g. 1 to 15 % by weight of a pigment and/or a dye, from 0 to 40 % by weight, e.g.
  • a binder (sticker /adhesion agent), optionally up to 5 % by weight, e.g. from 0.1 to 5 % by weight of a thickener, optionally from 0.1 to 2 % of an anti-foam agent, and optionally a preservative such as a biocide, antioxidant or the like, e.g. in an amount from 0.01 to 1 % by weight and a filler/vehicle up to 100 % by weight.
  • a binder sticker /adhesion agent
  • a preservative such as a biocide, antioxidant or the like
  • Seed Treatment formulations may additionally also comprise binders and optionally colorants.
  • Binders can be added to improve the adhesion of the active materials on the seeds after treatment.
  • Suitable binders are block copolymers EO/PO surfactants but also polyvinylalcoholsl, polyvinylpyrrolidones, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyleneimines (Lupasol®, Polymin®), polyethers, polyurethans, polyvinylacetate, tylose and copolymers derived from these polymers.
  • colorants can be included in the formulation.
  • Suitable colorants or dyes for seed treatment formulations are Rhodamin B, C.I. Pigment Red 112, C.I. Solvent Red 1 , pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
  • the invention also relates to seed comprising mixtures according to the present invention.
  • the amount of the compound I or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, more preferably from 1 g to 1000 g per 100 kg of seeds, most preferably from 1 g to 750 g per 100 kg of seeds, and in particular from 5 g to 500 g per 100 kg of seed.
  • the active compounds are prepared as a stock solution comprising 0.25% by weight of active compounds in acetone or DMSO. 1 % by weight of the emulsifier Uniperol® EL (wetting agent having emulsifying and dispersant action based on ethoxylated alkylphenols) is added to this solution, and the mixture is diluted with water to the desired concentration.
  • Uniperol® EL wetting agent having emulsifying and dispersant action based on ethoxylated alkylphenols
  • the efficacy (E) is calculated as follows using Abbot's formula:
  • ⁇ corresponds to the fungicidal infection of the treated plants in % and ⁇ corresponds to the fungicidal infection of the untreated (control) plants in %
  • An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants are not infected.
  • E x + y - x-y/100 E expected efficacy, expressed in % of the untreated control, when using the mixture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active compound A at the concentration a y efficacy, expressed in % of the untreated control, when using the active compound B at the concentration b
  • Example B.1a Fungicidal control of brown spot caused by Cochliobolus miyabeanus
  • Leaves of pot-grown rice seedlings are sprayed to run-off with an aqueous suspension containing a certain concentration of active ingredients prepared from a stock solution.
  • the plants are allowed to air-dry. At the following day the plants are inoculated with an aqueous spore suspension of Cochliobolus miyabeanus. Then the trial plants are immediately transferred to a humid chamber. After 6 days at 22-24O and a relative humidity close to 100 % the extent of fungal attack on the leaves is visually assessed as
  • test unit For evaluating control of vetch aphid (Megoura viciae) through contact or systemic means the test unit consists of 24-well-microtiter plates containing broad bean leaf disks. The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
  • test unit For evaluating control of boll weevil (Anthonomus grandis) the test unit consists of 24- well-microtiter plates containing an insect diet and 20-30 A. grandis eggs.
  • the mixtures are formulated using a solution containing 75 wt% water and 25 wt%
  • DMSO DMSO
  • Different concentrations of formulated mixtures are sprayed onto the insect diet at 20 ⁇ l, using a custom built micro atomizer at two replications.
  • microtiter plates After application the microtiter plates are incubated at 23 + 1 0 C, 50 +_ 5 % room humidity for 5 days. Egg and larval mortality is then visually assessed.
  • test unit For evaluating control of Mediterranean fruitfly (Ceratitis capitata) the test unit consists of 96-well-microtiter plates containing an insect diet and 50-80 C. capitata eggs. The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
  • DMSO DMSO
  • Different concentrations of formulated mixtures are sprayed onto the insect diet at 5 ⁇ l, using a custom built micro atomizer at two replications.
  • test unit For evaluating control of tobacco budworm (Heliothis virescens) the test unit consists of
  • the mixtures are formulated using a solution containing 75 wt% water and 25 wt%
  • microtiter plates were incubated at 28 + 1 0 C, 80 + 5 % room humidity for 5 days. Egg and larval mortality was then visually assessed.
  • the active compounds were formulated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide.
  • the stock solutions were mixed according to the given ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations.
  • MTP micro titer plate
  • a spore suspension of the pathogen to be treated was then added and after 7 days of inoculation, the MTP was measured using an absorption photometer.
  • the measured parameters were compared to the growth of the active compound-free control variant (100%) and the fungus-free and active compound-free blank value to determine the relative growth in % of the pathogens in the respective active compounds.
  • the visually determined percentages of infected leaf areas were converted into efficacies in % of the untreated control.
  • Test 1 Activity against the grey mold Botrytis cinerea in the microtiterplate test (Botrci) The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Botrci cinerea in an aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 1
  • the stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations.
  • MTP micro titer plate
  • a spore suspension of Phytophtora infestans containing a pea juice-based aqueous nutrient medium was then added.
  • the plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 2
  • the stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations.
  • MTP micro titer plate
  • a spore suspension of Septoria tritici in an aqueous biomalt solution was then added.
  • the plates were placed in a water vapor-saturated chamber at a temperature of 18°C.
  • the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 4

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The present invention relates to pesticidal mixtures comprising as active components 1 ) at least one cyanosulfoximine compound I of the formula ( I ) wherein R1, R2 and G are defined as in the description; and 2) at least one fungicidal compounds Il selected from azoles, strobilurins, carboxamides, carbamates, heterocyclic and various other compounds as defined in the description, in synergistically effective amounts. The invention relates further to methods and use of these mixtures for combating insects, arachnids or nematodes and harmful fungis in and on plants, and for protecting such plants being infested with pests, especially also for protecting seeds.

Description

Pesticidal mixtures comprising cyanosulfoximine compounds
The present invention relates to mixtures of active ingredients having synergistically enhanced action and to methods comprising applying said mixtures.
One typical problem arising in the field of pest control lies in the need to reduce the dosage rates of the active ingredient in order to reduce or avoid unfavorable environmental or toxicological effects whilst still allowing effective pest control.
Another problem encountered concerns the need to have available pest control agents which are effective against a broad spectrum of pests.
Another problem underlying the present invention is the desire for compositions that improve plants, a process which is commonly and hereinafter referred to as "plant health". For example, advantageous properties that may be mentioned are improved crop characteristics including: emergence, crop yields, protein content, more developed root system, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less fertilizers needed, less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, enhanced plant vigor, increased plant stand and early germination; or any other advantages familiar to a person skilled in the art. Methods for improving the health of plants by applying active compounds to the plants or the locus are a general need.
Another difficulty in relation to the use of pesticides is that the repeated and exclusive application of an individual pesticidal compound leads in many cases to a rapid selection of pests which have developed natural or adapted resistance against the active compound in question.
It is also an object of the present invention, with a view to reducing the application rates and broadening the activity spectrum of the active compounds I and II, to provide mixtures which, at a reduced total amount of active compounds applied, have improved activity against harmful fungi and animal pests.
It was therefore an object of the present invention to provide pesticidal mixtures which solve the problems outlined above.
The combating of harmful phytopathogenic fungi is in many regions not the only problem the farmer has to face. Also harmful insects can cause a great damage to crops and other plants. An efficient combination of fungicidal and insecticidal activity is desirable to overcome this problem. Thus, it is a further object of the present invention to provide a mixture which, on the one hand, has good fungicidal activity, and, on the other hand, good insecticidal activity, resulting in a broader pesticidal spectrum of action.
We have found that this object is in part or in whole achieved by the combination of active compounds defined as in the following.
The present invention relates to pesticidal mixtures comprising, as active compounds,
1 ) as active compound I at least one insecticidal compound of formula
Figure imgf000003_0001
formula (I)
wherein
is selected from
Figure imgf000003_0002
and wherein # denotes the bonding in formula I;
R1 is Cl or CF3 and
R2 is selected from hydrogen, chloro, CH3 or C2H5;
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers
and
2) as active compound Il at least one fungicidal compound selected from the groups I LA to 11. F: 11. A azoles such as triazoles, imidazoles, pyrazoles, thiazoles and oxazoles selected from the group consisting of azaconazole, benomyl, bitertanol, bromuconazole, carbendazim, cyproconazole, cyazofamid, difenoconazole, diniconazole, diniconazole-M, enilconazole, epoxiconazole, ethaboxam, etridiazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, fuberidazole, hexaconazole, hymexazole, imazalil, imazalil-sulfphate, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazol, paclobutrazol, pefurazoate, penconazole, prochloraz, propiconazole, prothioconazole, simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, thiabendazole, triticonazole, triflumizole, uniconazol and 1-(4-chloro- phenyl)-2-([1 ,2,4]triazol-1 -yl)-cycloheptanol;
11. B strobilurins selected from the group consisting of azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyribencarb, trifloxystrobin, methyl 2-(ortho-(2,5- dimethylphenyloxymethylene)phenyl)-3-methoxy-acrylate, 2-(2-(6-(3- chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2- methoxyimino-N-methyl-acetamide and 3-methoxy-2-(2-(N-(4- methoxy-phenyO-cyclo-propanecarboximidoylsulfanylmethyO-phenyl)- acrylic acid methyl ester;
11. C carboxamides selected from the group consisting of benalaxyl, benalaxyl-M, benodanil, bixafen, boscalid, carboxin, carpropamid, dimethomorph, diclocymet, fenhexamid, fluopyram, flutolanil, furametpyr, flumorph, flumetover, fluopicolide (picobenzamid), isopyrazam, mandipropamid, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, oxytetracyclin, penthiopyrad, silthiofam,thifluzamide, tiadinil, zoxamide, 5-fluoro-1 ,3-dimethyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,2-dimethyl- propyl)-phenyl]-amide, methyl-3-(4-chlorophenyl)- 3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)propionate, 2- chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide, N-(3-ethyl-3,5-5- trimethyl-cyclohexyl)-3-formylamino-2-hydroxy-benzamide, N-(2-{4-[3- (4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4- chlorophenyl)-prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- ethanesulfonylamino-3-methyl-butyramide, N-(6-methoxy-pyridin-3-yl) cyclopropane-carboxamide, 2-amino-4-methyl-thiazole-5- carboxamide, N-(2-cyanophenyl)-3,4-dichloroisothiazole-5- carboxamide, N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4- difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-chloro-3'- fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide,
N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4- difluoromethyl-2-methylthiazole-5-carboxamide, N-(3',4'-dichloro-4- fluorobiphenyl-2-yl)-3-difluoromethyl-1 -methylpyrazole-4- carboxamide, N-(3\4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl- 1-methylpyrazole-4-carboxamide; N-(3',4'-dichloro-4-fluorobiphenyl-2- yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide, N-(3\4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl- 1 -methylpyrazole-4-carboxamide, N-(2-(1 ,3-dimethylbutyl)-phenyl)-
1 ,3-dimethyl-5-fluoro-1 H-pyrazole-4-carboxamide, N-(4'-chloro-3',5- difluoro-biphenyl-2-yl)-3-difluoromethyl-1-methyl-1 H-pyrazole-4- carbox amide, N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3- trifluoromethyl-1-methyl-1 H-pyrazole-4-carbox amide, N-(3',4'- dichloro-5-fluoro-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl-1 H- pyrazole-4-carbox amide, N-(3',5-difluoro-4'-methyl-biphenyl-2-yl)-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-ca rboxamide,N-(3', 5-d ifluoro- 4'-methyl-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-(trans-2-bicyclopropyl-2-yl- phenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N- (2',4'-difluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole- 4- carboxamide, N-(2',4'-dichlorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',4'-difluorobiphenyl- 2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(2',4'- dichlorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2',5'-difluorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-(2',5'-dichlorobiphenyl- 2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',5'- difluorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2',5'-dichlorobiphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole- 4-carboxamide, N-(3',5'-difluorobiphenyl-2-yl)-1- methyl-3-trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-(3',5'- dichlorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole- 4- carboxamide, N-(3',5'-difluorobiphenyl-2-yl)-3-difluoromethyl-1 - methyl-1 H-pyrazole- 4-carboxamide, N-(3',5'-dichlorobiphenyl-2-yl)-3- difluoromethyl-1-methyl-I H-pyrazole- 4-carboxamide, N-(3'- fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3'-chlorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl- 1 H-pyrazole-4-carboxamide; N-(3'-fluorobiphenyl-2-yl)-3- difluoromethyl-1-methyl-1 H-pyrazole- 4-carboxamide, N-(3'- chlorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2'-fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H- pyrazole-4-carboxamide, N-(2'-chlorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2'-fluorobiphenyl-2-yl)- 3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-(2'- chlorbiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide; N-(2'-fluoro-4'-chloro-5'-methylbiphenyl-2-yl)-1-methyl- 3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4',5'- trifluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-1-methyl-3- difluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',4',5'- trifluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-chlorofluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-[2-(1 ,1 ,2,3,3,3- hexafluoropropoxy)phenyl]-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-[2-(1 ,1 , 2,3,3, 3-hexafluoropropoxy)-phenyl]-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-[2-(2-chloro- 1 ,1 ,2-trifluoroethoxy)phenyl]-1-methyl-3-trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-[2-(2-chlor-1 ,1 ,2-trifluoroethoxy)phenyl]- 3- difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-[2-(1 ,1 ,2,2- tetrafluoroethoxy)phenyl]-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-[2-(1 , 1 ,2,2-tetrafluoroethoxy)phenyl]-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'- (trifluoromethylthio)biphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxamide, N-(4'-(trifluoromethylthio)biphenyl-2-yl)-1 - methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide and N-(2- Bicycloprop-2-ylphenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide;
heterocyclic compounds selected from the group consisting of acibenzolar-S-methyl, anilazine, aldimorph, blasticidin-S, bupirimate, captafol, captan, chinomethionat, cyprodinil, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulphat, diflumetorim, dodemorph, dodemorph-acetate, famoxadone, fenamidone, fenarimol, ferimzone, fenpiclonil, fenpropidin, fenpropimorph, fludioxonil, fluazinam, fluoroimid, flutianil, folpet, fenoxanil, iprodione, mepanipyrim, nitrapyrin, nuarimol, octhilinone, oxolinic acid, piperalin, probenazole, procymidone, proquinazid, pyrifenox, pyrimethanil, pyroquilon, quinoxyfen, tricyclazole, triforine, tridemorph, vinclozolin, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)- [1 ,2,4]triazolo[1 ,5-a]pyτimidine, 6-(4-tert-butylphenyl)-5-methyl-
[1 ,2,4]triazolo[1 ,5-a]pyτimidine-7-ylamine, 5-methyl-6-(3,5,5-trimethyl- hexyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-ylamine, 5-methyl-6-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 6-methyl-5-octyl- [1 ,2,4]tri-azolo[1 ,5-a]pyrimidine-7-yl-amine, 6-ethyl-5-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 5-ethyl-6-octyl-
[1 ,2,4]triazolo[1 ,5-a]pyri-midine-7-ylamine, 5-ethyl-6-(3,5,5-trimethyl- hexyl)-[1 ,2,4]tri-azo-lo[1 ,5-a]pyrimi-dine-7-ylamine, 6-octyl-5-propyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 5-methoxy-methyl-6-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 6-octyl-5-trifluoromethyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine and 5-trifluoromethyl-6-
(3,5,5-trimethyl-hexyl)-[1 ,2,4]tri-azolo[1 ,5-a]pyrimidine-7-ylamine, 2,3,5,6-tetrachloro-4-methanesulfonyl-pyridine, 3,4,5-trichloro- pyridine-2,6-di-carbonitrile, N-(1-(5-bromo-3-chloro-pyridin-2-yl)- ethyl)-2,4-dichloro-nicotinamide, N-((5-bromo-3-chloro-pyridin-2-yl)- methyl)-2,4-dichloro-nicotinamide, 2-butoxy-6-iodo-3-propylchromen-
4-one and N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1- sulfonyl)-[1 ,2,4]triazole-1 -sulfonamide;
carbamates selected from the group consisting of diethofencarb, ferbam, flubenthiavalicarb, iprovalicarb, mancozeb, maneb, metam, methasulphocarb, metiram, propamocarb, propamocarb hydrochlorid,propineb, thiram, zineb, ziram, 4-fluorophenyl N-(1-(1-(4- cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, methyl 3-(4- chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate and carbamate oxime ethers of the formula
| |E 1
Figure imgf000007_0001
Z = N7 CH
various fungicides selected from the group of antibiotics comprising kasugamycin, kasugamycin-hydrochlorid-hydrat , mildiomycin, streptomycin, polyoxin and validamycin A; the group of nitrophenyl derivatives comprising binapacryl, dinocap, dinobuton, dicloran, nitrothal-isopropyl and tecnazen; the group of sulfur-containing heterocyclyl compounds comprising dithianon and isoprothiolane; the group of organometallic compounds comprising fentin salts; the group oforganophosphorus compounds comprising edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos and tolclofos-methyl; the group of organochlorine compounds comprising chlorothalonil, dichlofluanid, dichlorophen, pentachlorophenol and its salts, flusulfamide, hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate-methyl and tolylfluanid; the group of inorganic active compounds comprising Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, oxin-copper and sulfur; and/or selected from a group of various fungicides consisting of biphenyl, bronopol, cyflufenamid, cymoxanil, diphenylamine, dimethirimol, dodine, dodine free base, ethirimol, furalaxyl, iminoctadine, iminoctadine-triacetate, iminoctadine-tris(albesilate), guazatine, guazatine-acetate, metrafenone, prohexadione calcium, spiroxamine guanidine, N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfon-amide, N-(cyclopropylmethoxyimino-(6- difluoromethoxy-2,3-difluoro-phenyl)-methyl)-2-phenyl acetamide, N'- (4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl- N-methyl formamidine, N'-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5- dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'-(2-methyl-5- trifluormethyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine and N'-(5-difluormethyl-2-methyl-4-(3-trimethylsilanyl- propoxy)-phenyl)-N-ethyl-N-methyl formamidine;
in a synergistically effective amount.
The active compounds I of the formula I, their preparation and their action against insect and acarid pests have been described in WO 2006/060029 and in WO 2007/095229. Preparation methods of active compounds I of formula I can be found therein.
The active compounds Il mentioned above of groups II.A to II. F, their preparation and their action against harmful fungi are generally known (cf., for example, http://www.hclrss.demon.co.uk/index.html); they are commercially available. Benalaxyl, methyl N-(phenylacetyl)-N-(2,6-xylyl)-DL-alaninate (DE 29 03 612); metalaxyl, methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate (GB 15 00 581 ); ofurace, (RS)-α -(2-chloro-N-2,6-xylylacetamido)-γ -butyrolactone [CAS RN 58810-48-
3]; oxadixyl; N-(2,6-dimethylphenyl)-2-methoxy-N-(2-oxo-3-oxazolidinyl)acetamide (GB 20
58 059); aldimorph, " 4-alkyl-2,5(or 2,6)-dimethylmorpholine" , comprising 65-75% of 2,6- dimethylmorpholine and 25-35% of 2,5-dimethylmorpholine, comprising more than 85% of 4-dodecyl-2,5(or 2,6)-dimethylmorpholine, where " a l kyl" also includes octyl, decyl, tetradecyl and hexadecyl, with a cis/trans ratio of 1 :1 [CAS RN 91315-15-0]; dodine, 1-dodecylguanidinium acetate (Plant Dis. Rep., Vol. 41 , p.1029 (1957)); dodemorph, 4-cyclododecyl-2,6-dimethylmorpholine (DE-A1198125); fenpropimorph, (RS)-cis-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6- dimethylmorpholine (DE-A 27 52 096); fenpropidin, (RS)-I -[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine (DE-A 27 52 096); guazatine, mixture of the reaction products from the amidation of technical grade iminodi(octamethylene)diamine, comprising various guanidines and polyamines [CAS
RN 108173-90-6]; iminoctadine, 1 ,1 ' -iminodi(octamethylene)diguanidine (Congr. Plant Pathol., 1., p.27 (1968); spiroxamine, (8-tert-butyl-1 ,4-dioxaspiro[4.5]dec-2-yl)diethylamine (EP-A 281 842); tridemorph, 2,6-dimethyl-4-tridecylmorpholine (DE-A 1 1 64 152); pyrimethanil, 4,6-dimethylpyrimidin-2-ylphenylamine (DD-A 151 404); mepanipyrim, (4-methyl-6-prop-1-ynylpyrimidin-2-yl)phenylamine (EP-A 224 339); cyprodinil, (4-cyclopropyl-6-methylpyrimidin-2-yl)phenylamine (EP-A 310 550); cycloheximide, 4-{(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl}pi- peridine-2,6-dione [CAS RN 66-81-9]; griseofulvin, 7-chloro-2',4,6-trimethoxy-6'-methylspiro[benzofuran-2(3H),1 '-cyclohex-2'- ene]-3,4'-dione [CAS RN 126-07-8]; kasugamycin, 3-O-[2-amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-α -D- arabino-hexopyranosyl]-D-chiro-inositol [CAS RN 6980-18-3]; natamycin, (8E,14E,16E,18E,20E)-(1 R,3S,5R,7R,12R,22R,24S,25R,26S)-22-(3-amino-
3,6-dideoxy-β -D-mannopyranosyloxy)-1 ,3,26-trihydroxy-12-methyl-10-oxo-6,1 1 ,28- trioxatricyclo[22.3.1.057]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid [CAS RN 7681-93-8]; polyoxin, 5-(2-amino-5-O-carbamoyl-2-deoxy-L-xylonamido)-1 -(5-carboxy-1 ,2,3,4- tetrahydro-2,4-dioxopyrimidin-1-yl)-1 ,5-dideoxy-β -D-allofuranuronic acid [CAS RN
22976-86-9]; streptomycin, 1 ,1 '-{1-L-(1 ,3,5/2,4,6)-4-[5-deoxy-2-O-(2-deoxy-2-methylamino-α -L- glucopyranosyl)-3-C-formyl-α -L-lyxofuranosyloxy]-2,5,6-trihydroxycyclohex-1 ,3- ylene}diguanidine (J. Am. Chem. Soc. Vol. 69, p.1234 (1947)); bitertanol, β -([1 ,1'-biphenyl]-4-yloxy)-α -(1 ,1-dimethylethyl)-1 H-1 ,2,4-triazole-1-ethanol
(DE-A 23 24 020); bromuconazole, 1 -[[4-bromo-2-(2,4-dichlorophenyl)tetrahydro-2-furanyl]methyl]-1 H-
1 ,2,4-triazole (Proc. 1990 Br. Crop. Prot. Conf. - Pests Dis. Vol. 1 , p. 459); cyproconazole, 2-(4-chlorophenyl)-3-cyclopropyl-1-[1 ,2,4]triazol-1-ylbutan-2-ol
(US 4 664 696); difenoconazole, 1 -{2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-[1 ,3]dioxolan-2- ylmethylJ-1 H-[1 ,2,4]triazole (GB-A 2 098 607); diniconazole, (β E)-β -[(2,4-dichlorophenyl)methylene]-α -(1 ,1-dimethylethyl)-1 H-1 ,2,4- triazole-1-ethanol (Noyaku Kagaku, 1983, Vol. 8, p. 575); enilconazole (imazalil), 1-[2-(2,4-dichlorophenyl)-2-(2-propenyloxy)ethyl]-1 H-imidazole
(Fruits, 1973, Vol. 28, p. 545); epoxiconazole, (2RS,3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fluorophenyl)propyl]-
1 H-1 ,2,4-triazole (EP-A 196 038); fenbuconazole, α -[2-(4-chlorophenyl)ethyl]-α -phenyl-1 H-1 ,2,4-triazole-1- propanenitrile (Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. ,VoI. 1 , p. 33); fluquinconazole, 3-(2,4-dichlorophenyl)-6-fluoro-2-[1 ,2,4]- triazol-1 -yl-3H-quinazolin-4- one (Proc. Br. Crop Prot. Conf.-Pests Dis., 5-3, 41 1 (1992)); flusilazole, 1-{[bis(4-fluorophenyl)methylsilanyl]methyl}-1 H-[1 ,2,4]triazole (Proc. Br. Crop Prot. Conf.-Pests Dis., Vol. 1 , p.413 (1984)); flutriafol, α -(2-fluorophenyl)-α -(4-fluorophenyl)-1 H-1 ,2,4-triazole-1-ethanol (EP-A
15756); hexaconazole, 2-(2,4-dichlorophenyl)-1-[1 ,2,4]triazol-1-ylhexan-2-ol (CAS RN
79983-71-4); ipconazole, 2-[(4-chlorophenyl)methyl]-5-(1 -methylethyl)-1 -(1 H-1 ,2,4-triazol-1 -yl- methyl)cyclopentanol (EP-A 267 778), metconazole, 5-(4-chlorobenzyl)-2,2-dimethyl-1 -[1 ,2,4]triazol-1 -ylmethylcyclopentanol
(GB 857 383); myclobutanil, 2-(4-chlorophenyl)-2-[1 ,2,4]triazol-1-ylmethylpentanenitrile (CAS RN 88671- 89- 0); penconazole, 1-[2-(2,4-dichlorophenyl)pentyl]-1 H-[1 ,2,4]triazole (Pesticide Manual,
12th Ed. 2000, p. 712); propiconazole, 1 -[[2-(2,4-dichlorophenyl)-4-propyl-1 ,3-dioxolan-2-yl]methyl]-1 H-1 ,2,4- triazole (BE 835 579); prochloraz, N-(propyl-[2-(2,4,6-trichlorophenoxy)ethyl])imidazole-1-carboxamide (US 3
991 071 ); prothioconazole, 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4- dihydro[1 ,2,4]triazole-3-thione (WO 96/16048); simeconazole, α -(4-fluorophenyl)-α -[(trimethylsilyl)methyl]-1 H-1 ,2,4-triazole-1-ethanol [CAS RN 149508-90-7], tebuconazole, 1 -(4-chlorophenyl)-4,4-dimethyl-3-[1 ,2,4]triazol-1 -ylmethylpentan-3-ol (EP-A 40 345); tetraconazole, 1-[2-(2,4-dichlorophenyl)-3-(1 ,1 ,2,2-tetrafluoroethoxy)propyl]-1 H-1 ,2,4- triazole (EP-A 234 242); triadimefon, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1 H-1 ,2,4-triazol-1-yl)-2-butanone (BE 793 867); triadimenol, β -(4-chlorophenoxy)-α -(1 ,1-dimethylethyl)-1 H-1 ,2,4-triazole-1-ethanol
(DE-A 3 24 010); triflumizol, (4-chloro-2-trifluoromethylphenyl)-(2-propoxy-1 -[1 ,2,4]triazol-1 -ylethylidene)- amine (JP-A 79/119 462); triticonazole, (5E)-5-[(4-chlorophenyl)methylene]-2,2-dimethyl-1 -(1 H-1 ,2,4-triazol-1 - ylmethyl)cyclopentanol (FR 26 41 277); iprodione, N-isopropyl-3-(3,5-dichlorophenyl)-2,4-dioxoimidazolidine-1-carboxamide
(GB 13 12 536); myclozolin, (RS)-3-(3,5-dichlorophenyl)-5-methoxymethyl-5-methyl-1 ,3-oxazolidine-2,4- dione [CAS RN 54864-61 -8]; procymidone, N-(3,5-dichlorophenyl)-1 ,2-dimethylcyclopropane-1 ,2-dicarboximide (US
3 903 090); vinclozolin, 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione (DE-A 22 07
576); ferbam, iron(3+) dimethyldithiocarbamate (US 1 972 961 ); nabam, disodium ethylenebis(dithiocarbamate) (US 2 317 765); maneb, manganese ethylenebis(dithiocarbamate) (US 2 504 404); mancozeb, manganese ethylenebis(dithiocarbamate) polymer complex zinc salt (GB
996 264); metam, methyldithiocarbaminic acid (US 2 791 605); metiram, zinc ammoniate ethylenebis(dithiocarbamate) (US 3 248 400); propineb, zinc propylenebis(dithiocarbamate) polymer (BE 611 960); polycarbamate, bis(dimethylcarbamodithioato-κ S,κ S' )[μ -[[1 ,2- ethanediylbis[carbamodithioato-κ S,κ S' ]](2-)]]di[zinc] [CAS RN 64440-88-6]; thiram, bis(dimethylthiocarbamoyl) disulfide (DE-A 642 532); ziram, dimethyldithiocarbamate [CAS RN 137-30-4]; zineb, zinc ethylenebis(dithiocarbamate) (US 2 457 674); anilazine, 4,6-dichloro-N-(2-chlorophenyl)-1 ,3,5-triazine-2-amine (US 2 720 480); benomyl, N-butyl^-acetylaminobenzimidazole-i-carboxamide (US 3 631 176); boscalid, 2-chloro-N-(4'-chlorobiphenyl-2-yl)nicotinamide (EP-A 545 099); carbendazim, methyl (1 H-benzimidazol-2-yl)carbamate (US 3 657 443); carboxin, 5,6-dihydro-2-methyl-N-phenyl-1 ,4-oxathiine-3-carboxamide (US 3 249 499); oxycarboxin, 5,6-dihydro-2-methyl-1 ,4-oxathiine-3-carboxanilide 4,4-dioxide (US 3 399
214); cyazofamid, 4-chloro-2-cyano-N,N-dimethyl-5-(4-methylphenyl)-1 H-imidazole-1 -sulfonamide (CAS RN 120116-88-3]; dazomet, 3,5-dimethyl-1 ,3,5-thiadiazinane-2-thione (Bull. Soc. Chim. Fr. Vol. 15, p. 891
(1897)); diflufenzopyr, 2-{1-[4-(3,5-difluorophenyl)semicarbazono]ethyl}nicotinic acid [CAS RN
109293-97-2]; dithianon, 5,10-dioxo-5,10-dihydronaphtho[2,3-b][1 ,4]dithiin-2,3-dicarbonitrile (GB 857
383); famoxadone, (RS)-3-anilino-5-methyl-5-(4-phenoxyphenyl)-1 ,3-oxazolidine-2,4-dione
[CAS RN 131807-57-3]; fenamidone, (S)-1-anilino-4-methyl-2-methylthio-4-phenylimidazolin-5-one [CAS RN 161326-34-7]; fenarimol, α -(2-chlorophenyl)-α -(4-chlorophenyl)-5-pyrimidinemethanol (GB 12 18
623); fuberidazole, 2-(2-furanyl)-1 H-benzimidazole (DE-A 12 09 799); flutolanil, α ,α ,α -trifluoro-3'-isopropoxy-o-toluanilide (JP 1104514); furametpyr, 5-chloro-N-(1 ,3-dihydro-1 ,1 ,3-trimethyl-4-isobenzofuranyl)-1 ,3-dimethyl-1 H- pyτazole-4-carboxamide [CAS RN 123572-88-3]; isoprothiolane, diisopropyl 1 ,3-dithiolan-2-ylidenemalonate (Proc. Insectic. Fungic.
Conf. 8. Vol. 2, p. 715 (1975)); mepronil, 3'-isopropoxy-o-toluanilide (US 3 937 840); nuarimol, α -(2-chlorophenyl)-α -(4-fluorophenyl)-5-pyrimidinemethanol (GB 12 18
623); fluopicolide (picobenzamid), 2,6-dichloro-N-(3-chloro-5-trifluoromethylpyridin-2- ylmethyl)benzamide (WO 99/42447); probenazole, 3-allyloxy-1 ,2-benzothiazole 1 ,1 -dioxide (Agric. Biol. Chem. Vol. 37, p. 737 (1973)); proquinazid, 6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one (WO 97/48684); pyrifenox, 2',4'-dichloro-2-(3-pyridyl)acetophenone (EZ)-O-methyloxime (EP 49 854); pyroquilon, 1 ,2,5,6-tetrahydropyrrolo[3,2,1-ij]quinolin-4-one (GB 139 43 373) quinoxyfen, 5,7-dichloro-4-(4-fluorophenoxy)quinoline (US 5 240 940); silthiofam, N-allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide [CAS RN
175217-20-6]; thiabendazole, 2-(1 ,3-thiazol-4-yl)benzimidazole (US 3 017 415); thifluzamide, 2',6'-dibromo-2-methyl-4'-trifluoromethoxy-4-trifluoromethyl-1 ,3-thiazole-5- carboxanilide [CAS RN 130000-40-7]; thiophanate-methyl, 1 ,2-phenylenebis(iminocarbonothioyl)bis(dimethylcarbamate)
(DE-A 19 30 540); tiadinil, 3'-chloro-4,4'-dimethyl-1 ,2,3-thiadiazole-5-carboxanilide [CAS RN 223580-51-
6]; tricyclazole, 5-methyl-1 ,2,4-triazolo[3,4-b][1 ,3]benzothiazole [CAS RN 41814-78-2]; triforine, N, N' -{piperazine-1 ,4-diylbis[(trichloromethyl)methylene]}diformamide (DE-A 19 01 421 ); 5-chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5- a]pyrimidine (WO 98/46607) and other triazolo pyrimidine (EP-A 71 792; EP-A 141
317; WO 2003/009687; WO 2005/087771 ; WO 2005/087772; WO 2005/087773; WO
2006/087325; WO 2006/092428); Bordeaux mixture, mixture of CuSO4 x 3Cu(OH)2 x 3CaSO4 [CAS RN 8011-63-0] copper acetate, Cu(OCOCHs)2 [CAS RN 8011-63-0]; copper oxychloride, Cu2CI(OH)3 [CAS RN 1332-40-7]; basic copper sulfate, CuSO4 [CAS RN 1344-73-6]; binapacryl, (RS)-2-sec-butyl-4,6-dinitrophenyl 3-methylcrotonate [CAS RN 485-31-4]; dinocap, mixture of 2,6-dinitro-4-octylphenylcrotonate and 2,4-dinitro-6- octylphenylcrotonate, where "octyl" is a mixture of 1-methylheptyl, 1-ethylhexyl and 1- propylpentyl (US 2 526 660); dinobuton, (RS)-2-sec-butyl-4,6-dinitrophenyl isopropyl carbonate [CAS RN 973-21-7]; nitrothal-isopropyl, diisopropyl 5-nitroisophthalate (Proc. Br. Insectic. Fungic. Conf. 7., Vol. 2, p. 673 (1973)); fenpiclonil, 4-(2,3-dichlorophenyl)-1 H-pyrrole-3-carbonitrile (Proc. 1988 Br. Crop Prot.
Conf. - Pests Dis., Vol. 1 , p. 65); fludioxonil, 4-(2,2-difluorobenzo[1 ,3]dioxol-4-yl)-1 H-pyrrole-3-carbonitrile (The Pesticide
Manual, publ. The British Crop Protection Council, 10th ed. 1995, p. 482); acibenzolar-S-methyl, methyl 1 ,2,3-benzothiadiazole-7-carbothioate [CAS RN 135158-
54-2]; flubenthiavalicarb (benthiavalicarb), isopropyl {(S)-1-[(1 R)-1-(6-fluorobenzothiazol-2-yl)- ethylcarbamoyl]-2-methylpropyl}carbamate (JP-A 09/323 984); carpropamid, 2,2-dichloro-N-[1 -(4-chlorophenyl)ethyl]-1 -ethyl-3-methylcyclopropane- carboxamide [CAS RN 104030-54-8]; chlorothalonil, 2,4,5,6-tetrachloroisophthalonitrile (US 3 290 353); cyflufenamid, (Z)-N-[α -(cyclopropylmethoxyimino)-2,3-difluoro-6-
(trifluoromethyl)benzyl]-2-phenylacetamide (WO 96/19442); cymoxanil, 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (US 3 957 847); diclomezine, 6-(3,5-dichlorophenyl-p-tolyl)pyridazin-3(2H)-one (US 4 052 395) diclocymet, (RS)-2-cyano-N-[(R)-1-(2,4-dichlorophenyl)ethyl]-3,3-dimethylbutyramide
[CAS RN 139920-32-4]; diethofencarb, isopropyl 3,4-diethoxycarbanilate (EP-A 78 663); edifenphos, O-ethyl S,S-diphenyl phosphorodithioate (DE-A 14 93 736) ethaboxam, N-(cyano-2-thienylmethyl)-4-ethyl-2-(ethylamino)-5-thiazolecarboxamide
(EP-A 639 574); fenhexamid, N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide
(Proc. Br. Crop Prot. Conf. - Pests Dis., 1998, Vol. 2, p. 327); fentin-acetate, triphenyltin (US 3 499 086); fenoxanil, N-(1-cyano-1 ,2-dimethylpropyl)-2-(2,4-dichlorophenoxy)propanamide (EP-A 262 393); ferimzone, (Z)-2'-methylacetophenone-4,6-dimethylpyrimidin-2-ylhydrazone [CAS RN
89269-64-7]; fluazinam, S-chloro-N-tS-chloro^^-dinitro^-^rifluoromethyOphenyO-S-^rifluoromethyl)- 2-pyridinamine (The Pesticide Manual, publ. The British Crop Protection Council, 10th ed. (1995), p. 474); fosetyl, fosetyl-aluminum, ethylphosphonate (FR 22 54 276); iprovalicarb, isopropyl [(1 S)-2-methyl-1 -(1 -p-tolylethylcarbamoyl)propyl]carbamate
(EP-A 472 996); hexachlorobenzene (C. R. Seances Acad. Agric. Fr., Vol. 31 , p. 24 (1945)); mandipropamid, (RS)-2-(4-chlorophenyl)-N-[3-methoxy-4-(prop-2-ynyloxy)phenethyl]-2-
(prop-2-ynyloxy)acetamide (WO 03/042166); metrafenone, 3'-bromo-2,3,4,6'-tetramethoxy-2',6-dimethylbenzophenone (US 5 945
567); pencycuron, 1-(4-chlorobenzyl)-1-cyclopentyl-3-phenylurea (DE-A 27 32 257); penthiopyrad, (RS)-N-[2-(1 ,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1 H- pyrazole-4-carboxamide (JP 10/130268); propamocarb, isopropyl 3-(dimethylamino)propylcarbamate (DE-A 15 67 169); phthalide (DE-A 16 43 347); toloclofos-methyl, 0-2,6-dichloro-p-tolyl O,O-dimethyl phosphorothioate (GB 14 67
561 ); quintozene, pentachloronitrobenzene (DE-A 682 048); zoxamide, (RS)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-p-toluamide
[CAS RN 156052-68-5]; captafol, N-(1 ,1 ,2,2-tetrachloroethylthio)cyclohex-4-ene-1 ,2-dicarboximide
(Phytopathology, Vol. 52, p. 754 (1962)); captan, N-(trichloromethylthio)cyclohex-4-ene-1 ,2-dicarboximide (US 2 553 770); dichlofluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-phenylsulfamide (DE-A 1 1 93
498); folpet, N-(trichloromethylthio)phthalimide (US 2 553 770); tolylfluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-p-tolylsulfamide (DE-A 1 1 93
498); dimethomorph, 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-yl- propenone (EP-A 120 321 ); flumetover, 2-(3,4-dimethoxyphenyl)-N-ethyl-α ,α ,α -trifluoro-N-methyl-p-toluamide
[AGROW no. 243, 22 (1995)]; flumorph, 3-(4-fluorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylpropenone
(EP-A 860 438);
N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-
(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide (WO 03/66610);
N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4- carboxamide and N-(3\4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-
1-methylpyrazole-4-carboxamide (WO 03/70705); N-(2-cyanophenyl)-3,4-dichloroisothiazole-5-carboxamide (WO 99/24413);
N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2- methanesulfonylamino-3-methylbutyramide, N-(2-(4-[3-(4-chlorophenyl)prop-2- ynyloxy]-3-methoxyphenyl)ethyl)-2-ethanesulfonylamino-3-methylbutyramide (WO
04/49804); N-(2-Bicycloprop-2-ylphenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide is a mixture of the diastereomers N-(trans-2-bicycloprop-2-ylphenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide and N-(cis-2-bicycloprop-2-ylphenyl)-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide (WO 03/074491 and WO
2006/015866);
3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine (EP-A 10 35 122);
2-butoxy-6-iodo-3-propylchromen-4-one (WO 03/14103);
N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-[1 ,2,4]triazole-1- sulfonamide (EP-A 10 31 571 ); methyl (2-chloro-5-[1 -(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1 -(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate (EP-A
12 01 648); methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3- methylbutyrylamino)propionate (EP-A 10 28 125); azoxystrobin, methyl 2-{2-[6-(2-cyano-1-vinylpenta-1 ,3-dienyloxy)pyrimidin-4- yloxy]phenyl}-3-methoxyacrylate (EP-A 382 375), dimoxystrobin, (E)-2-(methoxyimino)-N-methyl-2-[α -(2,5-xylyloxy)-o-tolyl]acetamide
(EP-A 477 631 ); fluoxastrobin, (E)-{2-[6-(2-chlorophenoxy)-5-fluoropyrimidin-4-yloxy]phenyl}(5,6- dihydro-1 ,4,2-dioxazin-3-yl)methanone O-methyloxime (WO 97/27189); kresoxim-methyl, methyl (E)-methoxyimino[α -(o-tolyloxy)-o-tolyl]acetate (EP-A 253
213); metominostrobin, (E)-2-(methoxyimino)-N-methyl-2-(2-phenoxyphenyl)acetamide
(EP-A 398 692); orysastrobin, (2E)-2-(methoxyimino)-2-{2-[(3E,5E,6E)-5-(methoxyimino)-4,6-dimethyl-
2,8-dioxa-3,7-diazanona-3,6-dien-1 -yl]phenyl}-N-methylacetamide (WO 97/15552); picoxystrobin, methyl 3-methoxy-2-[2-(6-trifluoromethylpyridin-2- yloxymethyl)phenyl]acrylate (EP-A 278 595); pyraclostrobin, methyl N-{2-[1-(4-chlorophenyl)-1 H-pyrazol-3-yloxymethyl]phenyl}(N- methoxy)carbamate (WO 96/01256); trifloxystrobin, methyl (E)-methoxyimino-{(E)-α -[1-(α ,α ,α -trifluoro-m- tolyl)ethylideneaminooxy]-o-tolyl}acetate (EP-A 460 575); methyl 2-[ortho-(2,5-dimethylphenyloxymethylene)phenyl]-3-methoxyacrylate (EP-A
226 917); 5-chloiO-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyri- midine (WO 98/46608);
3,4-dichloro-N-(2-cyanophenyl)isothiazole-5-carboxamide (WO 99/24413), compounds of the formula III (WO 04/049804);
N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2- methanesulfonylamino-3-methylbutyramide and N-(2-(4-[3-(4-chlorophenyl)prop-2- ynyloxy]-3-methoxyphenyl)ethyl)-2-ethanesulfonylamino-3-methylbutyramide (WO
03/66609);
2-butoxy-6-iodo-3-propylchromen-4-one (WO 03/14103);
N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-[1 ,2,4]triazole-1- sulfonamide (WO 03/053145); methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)- propanoate (EP-A 1028125).
We have accordingly found that several objects can be achieved by the mixtures, defined at the outset, of the active compounds I and II. Moreover, we have found that simultaneous, that is joint or separate, application of at least one compound I and at least one of the active compounds Il or successive application of at least one of the compound(s) I and at least one of the active compounds Il allows better control of harmful fungi than is possible with the individual compounds alone (synergistic mixtures).
Moreover, the present invention relates to: agricultural compositions comprising a mixture of at least one active compound I and at least one active compound II; - the use of a mixture of at least one active compound I and at least one active compound Il for combating animal pests; the use of a mixture of at least one active compound I and at least one active compound Il for combating phytopathogenic harmful fungi; a method of combating animal pests which comprises contacting the animal pests, their habit, breeding ground, food supply, plant, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal attack or infestation with a pesticidally effective amount of a mixture of at least one active compound I and at least one active compound II; a method for protecting crops from attack or infestation by animal pests and/or phythopathogenic harmful fungi, which comprises contacting a crop with a mixture of at least one active compound I and at least one active compound II; a method for the protection of seeds from soil insects and of the seedlings' roots and shoots from soil and foliar insects and/or phythopathogenic harmful fungi comprising contacting the seeds before sowing and/or after pregermination with a mixture of at least one active compound I and at least one active compound II; and seeds comprising a mixture of at least one active compound I and at least one active compound II.
The compounds I can be used as synergists for a large number of different fungicidal active compounds. By simultaneous, that is joint or separate, application of compound(s) I with at least one active compound II, the fungicidal and/or insecticidal activity is increased in a superadditive manner.
The compounds I can be present in different crystal modifications, which may differ in biological activity.
Preferences
Preferences of insecticidal cyanosulfoximine compound I of formula I
With regard to their use in the pesticidal mixtures of the present invention, active compounds I of formula I are preferred, wherein
R1 is CF3
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers.
With regard to their use in the pesticidal mixtures of the present invention, active compounds I of formula I are preferred, wherein
R1 is Cl
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers.
With regard to their use in the pesticidal mixtures of the present invention, active compounds I of formula I are preferred, wherein G is G1 and
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers.
With regard to their use in the pesticidal mixtures of the present invention, active compounds I of formula I are also preferred, wherein
G is G1 and
R2 is hydrogen, chloro, or C2H5;
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers.
With regard to their use in the pesticidal mixtures of the present invention, active compounds I of formula I are also preferred, wherein
G is G2 and
R2 is hydrogen
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enantiomers and/or diastereomers.
Preferred insectidal cyanosulfoximine compound I of formula I are given in the following table:
Table d:
Figure imgf000018_0001
Figure imgf000019_0001
The compounds of formula I include racemic mixtures, individual pure enantiomers and diasteroemers and optically active mixtures.
Preference is given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group II.A of the azoles.
Preference is also given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group II. B of the strobilurins.
Preference is given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group II. C of the carboxamides.
Preference is furthermore also given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group 11. D of the heterocyclic compounds.
Preference is furthermore also given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group II. E of the carbamates.
Preference is furthermore also given to mixtures of a compound of the formula I in table C.I with at least one active compound selected from the group II. F of other various fungicides.
Preferences of fungicidal compound Il
Preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II.A of azoles consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl, carbendazim and ethaboxam.
Particular preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II.A of azoles consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, propiconazole, prothioconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl and carbendazim.
Very particular preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II.A of azoles consisting of benomyl, carbendazim, , epoxiconazole, fluquinconazole, flutriafol, flusilazole, metconazole, prochloraz, prothioconazole, tebuconazole and triticonazole.
Preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group of the II. B of strobilurins consisting of azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin and trifloxystrobin.
Particular preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group 11. B of strobilurins consisting of azoxystrobin, kresoxim-methyl, orysastrobin and pyraclostrobin.
Very particular preference is given to mixtures of a compound of the formula I with pyraclostrobin.
Preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. C of carboxamides consisting of bixafen, boscalid, carpropamid, dimethomorph, fenhexamid, flumorph, fluopicolide (picobenzamid), fluopyram, isothianil, mandipropamid, metalaxyl, mefenoxam, ofurace, penthiopyrad and zoxamide. Particular preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. C of carboxamides consisting of boscalid, carpropamid, dimethomorph, fenhexamid, fluopicolide, fluopyram, mandipropamid, metalaxyl, mefenoxam, ofurace, penthiopyrad and zoxamide.
Very particular preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. C of carboxamides consisting of boscalid, dimethomorph and penthiopyrad.
Preference is given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. D of heterocyclic compounds consisting of acibenzolar-S-methyl, captafol, cyprodinil, dodemorph, famoxadone fenamidone, fenarimol, fenpropimorph, fenpropidin, fenoxanil, fludioxonil, fluazinam, folpet, iprodione, mepanipyrim, probenazole, proquinazid, pyrimethanil, quinoxyfen triforine, tridemorph, vinclozolin and 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)- [1 ,2,4]triazolo[1 ,5-a]pyrimidine.
Particular preference is also given to mixtures of a compound of the formula I with at least one active compound Il selected from the group 11. D of heterocyclic compounds consisting of dodemorph, famoxadone, fenpropimorph, iprodione, proquinazid , pyrimethanil, quinoxyfen, tridemorph, vinclozolin and 5-chloro-7-(4-methylpiperidin-1- yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine.
Very particular preference is given to mixtures mixtures of a compound of the formula I with at least one active compound Il selected from the group 11. D of heterocyclic compounds consisting of dodemorph, famoxadone, fenpropimorph, proquinazid pyrimethanil, tridemorph and 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6- trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine.
Preference is also given to mixtures of a compound of the formula I with at least one active compound Il selected from the group 11. E of carbamates consisting of iprovalicarb, flubenthiavalicarb, maneb, mancozeb, metiram, propineb, propamocarb and thiram.
Particular preference is also given to mixtures of a compound of the formula I with at least one active compound Il selected from the group 11. E of carbamates consisting of iprovalicarb, flubenthiavalicarb, maneb, mancozeb, metiram and thiram.
Very particular preference is given to mixtures mixtures of a compound of the formula I with at least one active compound Il selected from the group II. E of carbamates consisting of maneb, mancozeb, metiram and thiram. Preference is also given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. F of other fungicides consisting of chlorothalonil, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, cymoxanil, dichlofluanid, dithianon, fentin salts, such as fentin acetate, fosetyl, fosetyl-aluminum, flusulfamide, metrafenone, phosphorous acid and its salts, thiophanate-methyl, sulfur and spiroxamine.
Particular preference is also given to mixtures of a compound of the formula I with at least one active compound Il selected from the group II. F of other fungicides consisting of chlorothalonil, dithianon, flusulfamide, fosetyl-aluminium, metrafenone, phosphorous acid and its salts and thiophanate-methyl.
Very particular preference is given to mixtures mixtures of a compound of the formula I with at least one active compound Il selected from the group II. F of other fungicides consisting of chlorothalonil, dithianon, flusulfamide, metrafenone and phosphorous acid and its salts.
Preferred combinations of insecticidal compound I with fungicidal compound Il
High Preference is given to the following combinations of insecticidal compounds I with fungicidal compounds Il in tables A to F.
Table A
Preferred combinations of preferred insecticidal compound I with preferred fungicidal compound Il of group 11. A:
Figure imgf000022_0001
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001
Figure imgf000029_0001
Table B
Preferred combinations of preferred insecticidal compound I with preferred fungicidal compound Il of group II. B:
Figure imgf000029_0002
Figure imgf000030_0001
Table C
Preferred combinations of preferred insecticidal compound I with preferred fungicidal
Figure imgf000030_0002
Figure imgf000031_0001
Figure imgf000032_0001
Table D
Preferred combinations of preferred insecticidal compound I with preferred fungicidal compound Il of group II. D:
Figure imgf000032_0002
Figure imgf000033_0001
Figure imgf000034_0001
Figure imgf000035_0001
Figure imgf000036_0001
Figure imgf000037_0001
Figure imgf000038_0001
Table E
Preferred combinations of preferred insecticidal compound I with preferred fungicidal compound Il of group II. E:
Figure imgf000038_0002
Figure imgf000039_0001
Figure imgf000040_0001
Figure imgf000041_0001
Table F
Preferred combinations of preferred insecticidal compound I with preferred fungicidal compound Il of group II. F:
Figure imgf000041_0002
Figure imgf000042_0001
Figure imgf000043_0001
Figure imgf000044_0001
Figure imgf000045_0001
Pests and fungi
The mixtures of the present invention have excellent activity against a broad spectrum of phytopathogenic fungi and animal pests.
Animal pests The mixtures of the present invention have excellent activity against a broad spectrum of animal pests.
They are in particular suitable for efficiently controlling arthropodal pests such as arachnids, myriapedes and insects as well as nematodes.
In particular, they are suitable for controlling insect pests, such as insects from the order of
lepidopterans (Lepidoptera), for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, HeIIuIa undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni and Zeiraphera canadensis;
beetles (Coleoptera), for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Aphthona euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Ctenicera ssp., Diabrotica longicornis, Diabrotica semipunctata, Diabrotica 12-punctata Diabrotica speciosa, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, lps typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllobius pyri, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus and Sitophilus granaria;
flies, mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Contarinia sorghicola Cordylobia anthropophaga, Culicoides furens, Culex pipiens, Culex nigripalpus, Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta melanura, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia antique, Delia coarctata, Delia platura, Delia radicum, Dermatobia hominis, Fannia canicularis, Geomyza Tripunctata, Gasterophilus intestinalis, Glossina morsitans, Glossina palpalis, Glossina fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia platura, Hypoderma lineata, Leptoconops torrens, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mansonia titillanus, Mayetiola destructor, Musca autumnalis, Musca domestica, Muscina stabulans, Oestrus ovis, Opomyza florum, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Phlebotomus argentipes, Psorophora columbiae, Psila rosae, Psorophora discolor, Prosimulium mixtum, Rhagoletis cerasi, Rhagoletis pomonella, Sarcophaga haemorrhoidalis, Sarcophaga spp., Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and Tabanus similis, Tipula oleracea, and Tipula paludosa;
thrips (Thysanoptera), e.g. Dichromothrips corbetti, Dichromothrips ssp., Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci,
termites (Isoptera), e.g. Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Reticulitermes santonensis, Reticulitermes grassei, Termes natalensis, and Coptotermes formosanus;
cockroaches (Blattaria - Blattodea), e.g. Blattella germanica, Blattella asahinae, Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis;
bugs, aphids, leafhoppers, whiteflies, scale insects, cicadas (Hemiptera), e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus,
Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis , Thyanta perditor, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spiraecola, Aphis sambuci, Acyrthosiphon pisum, Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui, Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus prunicola, Brevicoryne brassicae, Capitophorus horni, Cerosipha gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Dysaphis plantaginea, Dysaphis pyri, Empoasca fabae, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Melanaphis pyrarius, Metopolophium dirhodum, Myzus persicae, Myzus ascalonicus, Myzus cerasi, Myzus varians, Nasonovia ribis- nigri, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalosiphum insertum, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Sitobion avenae, Trialeurodes vaporariorum, Toxoptera aurantiiand, Viteus vitifolii, Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., and Arilus critatus;
ants, bees, wasps, sawflies (Hymenoptera), e.g. Athalia rosae, Atta cephalotes, Atta capiguara, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Lasius niger, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta, Solenopsis richteri, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla occidentalis, Bombus spp., Vespula squamosa, Paravespula vulgaris, Paravespula pennsylvanica, Paravespula germanica, Dolichovespula maculata, Vespa crabro, Polistes rubiginosa, Camponotus floridanus, and Linepithema humile;
crickets, grasshoppers, locusts (Orthoptera), e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Hieroglyphus daganensis, Kraussaria angulifera, Calliptamus italicus, Chortoicetes terminifera, and Locustana pardalina;
arachnoidea, such as arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and
Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Ambryomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor andersoni, Dermacentor variabilis, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi, Ornithodorus turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp. such as Aculus schlechtendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp. such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp. such as Brevipalpus phoenicis; Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and Oligonychus pratensis; Araneida, e.g. Latrodectus mactans, and Loxosceles reclusa;
fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephalides canis, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus,
silverfish, firebrat (Thysanura), e.g. Lepisma saccharina and Thermobia domestica,
centipedes (Chilopoda), e.g. Scutigera coleoptrata,
millipedes (Diplopoda), e.g. Narceus spp.,
Earwigs (Dermaptera), e.g. forficula auricularia,
lice (Phthiraptera), e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus.
Collembola (springtails), e.g. Onychiurus ssp..
They are also suitable for controlling Nematodes : plant parasitic nematodes such as root knot nematodes, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, and other Meloidogyne species; cyst-forming nematodes, Globodera rostochiensis and other Globodera species; Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, and other Heterodera species; Seed gall nematodes, Anguina species; Stem and foliar nematodes, Aphelenchoides species; Sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; Pine nematodes, Bursaphelenchus xylophilus and other Bursaphelenchus species; Ring nematodes, Criconema species, Criconemella species, Criconemoides species, Mesocriconema species; Stem and bulb nematodes, Ditylenchus destructor, Ditylenchus dipsaci and other Ditylenchus species; AwI nematodes, Dolichodorus species; Spiral nematodes, Heliocotylenchus multicinctus and other Helicotylenchus species; Sheath and sheathoid nematodes, Hemicycliophora species and Hemicriconemoides species; Hirshmanniella species; Lance nematodes, Hoploaimus species; false rootknot nematodes, Nacobbus species; Needle nematodes, Longidorus elongatus and other Longidorus species; Lesion nematodes, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus, Pratylenchus goodeyi and other Pratylenchus species; Burrowing nematodes, Radopholus similis and other Radopholus species; Reniform nematodes, Rotylenchus robustus and other Rotylenchus species; Scutellonema species; Stubby root nematodes, Trichodorus primitivus and other Trichodorus species, Paratrichodorus species; Stunt nematodes, Tylenchorhynchus claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus species; Citrus nematodes, Tylenchulus species; Dagger nematodes, Xiphinema species; and other plant parasitic nematode species.
They are also useful for controlling arachnids (Arachnoidea), such as acarians (Acarina), e.g. of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp. such as Aculus schlechtendali, Phyllocoptrata oleivora and Eriophyes sheldoni; Tarsonemidae spp. such as Phytonemus pallidus and Polyphagotarsonemus latus; Tenuipalpidae spp. such as Brevipalpus phoenicis; Tetranychidae spp. such as
Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and oligonychus pratensis.
Phytopathogenic fungi
The mixtures of the present invention have excellent activity against a broad spectrum of phytopathogenic fungi Ascomycetes, Basidiomycetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). Some of them are systemically effective and can be employed in crop protection as foliar fungicides, as fungicides for seed dressing and as soil fungicides. They can also be used for treating seed.
They are particularly important in the control of a multitude of fungi on various cultivated plants, such as wheat, rye, barley, oats, rice, corn, lawns, bananas, cotton, soybean, coffee, sugar cane, grapevines, fruits and ornamental plants, and vegetables such as cucumbers, beans, tomatoes, potatoes and cucurbits, and on the seeds of these plants.
They are especially suitable for controlling the following plant diseases:
Alternaria species on vegetables, oilseed rape, sugar beet and fruit and rice, for example, A. solani or A. alternata on potatoes and tomatoes;
Aphanomyces species on sugar beet and vegetables;
Ascochyta species on cereals and vegetables;
Bipolaris and Drechslera species on corn, cereals, rice and lawns, for example,
D. maydis on corn; - Blumeria graminis (powdery mildew) on cereals;
Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and grapevines;
Bremia lactucae on lettuce;
Cercospora species on corn, soybeans, rice and sugar beet;
Cochliobolus species on corn, cereals, rice, for example Cochliobolus sativus on cereals, Cochliobolus miyabeanus on rice;
Colletotricum species on soybeans and cotton;
Drechslera species, Pyrenophora species on corn, cereals, rice and lawns, for example, D. teres on barley or D. tritici-repentis on wheat;
Esca on grapevines, caused by Phaeoacremonium chlamydosporium, Ph. Aleophilum and Formitipora punctata (syn. Phellinus punctatus);
Exserohilum species on corn;
Erysiphe cichoracearum and Sphaerotheca fuliginea on cucumbers;
Fusarium and Verticillium species on various plants, for example, F graminearum or F. culmorum on cereals or F. oxysporum on a multitude of plants, such as, for example, tomatoes;
Gaeumanomyces graminis on cereals;
Gibberella species on cereals and rice (for example Gibberella fujikuroi on rice);
Grainstaining complex on rice;
Helminthosporium species on corn and rice; - Michrodochium nivale on cereals;
Mycosphaerella species on cereals, bananas and peanuts, for example, M. graminicola on wheat or M.fijiensis on bananas;
Peronospora species on cabbage and bulbous plants, for example, P. brassicae on cabbage or P. destructor on onions; - Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans;
Phomopsis species on soybeans and sunflowers;
Phytophthora infestans on potatoes and tomatoes;
Phytophthora species on various plants, for example, P. capsici on bell pepper;
Plasmopara viticola on grapevines; - Podosphaera leucotricha on apples;
Pseudocercosporella herpotrichoides on cereals; Pseudoperonospora on various plants, for example, P. cubensis on cucumber or
P. humili on hops;
Puccinia species on various plants, for example, P. triticina, P. striformins, P. hordei or P.graminis on cereals or P. asparagi on asparagus; - Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S.attenuatum,
Entyloma oryzae on rice;
Pyricularia grisea on lawns and cereals;
Pythium spp. on lawns, rice, corn, cotton, oilseed rape, sunflowers, sugar beet, vegetables and other plants, for example, P. ultiumum on various plants, P. aphanidermatum on lawns;
Rhizoctonia species on cotton, rice, potatoes, lawns, corn, oilseed rape, sugar beet, vegetables and on various plants, for example, R. solani on beet and various plants;
Rhynchosporium secalis on barley, rye and triticale; - Sclerotinia species on oilseed rape and sunflowers;
Septoria tritici and Stagonospora nodorum on wheat;
Erysiphe (syn. Uncinula) necator on grapevines;
Setospaeria species on corn and lawns;
Sphacelotheca reilinia on corn; - Thievaliopsis species on soybeans and cotton;
Tilletia species on cereals;
Ustilago species on cereals, corn and sugar cane, for example, U. maydis on corn;
Venturia species (scab) on apples and pears, for example, V. inaequalis on apples.
The mixtures according to the invention are also suitable for controlling harmful fungi in the protection of materials (for example wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products. In the protection of wood, particular attention is paid to the following harmful fungi: Ascomycetes, such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes, such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp. and Tyromyces spp., Deuteromycetes, such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes, such as Mucor spp., additionally in the protection of materials the following yeasts: Candida spp. and Saccharomyces cerevisae.
Formulations
The pesticidal mixtures according to the present invention can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compounds according to the invention.
The formulations are prepared in a known manner (see e.g. for review US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO 91/13546, US 4,172,714, US 4,144,050, US 3,920,442, US 5,180,587, US 5,232,701 , US 5,208,030, GB 2,095,558, US 3,299,566, Klingman, Weed Control as a Science, John Wiley and
Sons, Inc., New York, 1961 , Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, A., Formulation technology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001 , 2. D. A. Knowles, Chemistry and Technology of Agrochemical Formulations, Kluwer Academic Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by extending the active corn-pound with auxiliaries suitable for the formulation of agrochemicals, such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, antifoaming agents, anti-freezing agents, for seed treatment formulation also optionally gelling agents.
Examples of suitable solvents are water, aromatic solvents (for example Solvesso™ products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP(N-methyl-pyrrolidone), NOP (N-octyl- pyrrolidone)), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used.
Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates).
Examples of dispersants are lignin-sulfite waste liquors and methylcellulose.
Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalene- sulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropyl-ene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.
Substances, which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
Also anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.
Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate.
A suitable preservative is e.g. dichlorophen.
An example of a gelling agent is carrageen (Satiagel®)
Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compounds. In this case, the active compounds are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight (according to NMR spectrum or HLPC spectrum). For seed treatment purposes, respective formulations can be diluted 2-10 fold leading to concentrations in the ready to use preparations of 0,01 to 60% by weight active compounds by weight, preferably 0,1 to 40% by weight.
The mixtures of the present invention can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention.
Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 % per weight.
The active compound(s) may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
The following are examples of formulations:
1. Products for dilution with water for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.
A) Water-soluble concentrates (SL, LS)
10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound(s) dissolve(s) upon dilution with water, whereby a formulation with 10 % (w/w) of active compound(s) is obtained.
B) Dispersible concentrates (DC) 20 parts by weight of the active compound(s) are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compound(s) is obtained.
C) Emulsifiable concentrates (EC)
15 parts by weight of the active compound(s) are dissolved in 7 parts by weight of xy- lene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion, whereby a formulation with 15% (w/w) of active compound(s) is obtained.
D) Emulsions (EW, EO, ES)
25 parts by weight of the active compound(s) are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound(s) is obtained.
E) Suspensions (SC, OD, FS)
In an agitated ball mill, 20 parts by weight of the active compound(s) are comminuted with addition of 10 parts by weight of dispersants, wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound(s) suspension. Dilution with water gives a stable suspension of the active compound(s), whereby a formulation with 20% (w/w) of active compound(s) is obtained.
F) Water-dispersible granules and water-soluble granules (WG, SG)
50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluid- ized bed). Dilution with water gives a stable dispersion or solution of the active compound^), whereby a formulation with 50% (w/w) of active compound(s) is obtained.
G) Water-dispersible powders and water-soluble powders (WP, SP, SS, WS) 75 parts by weight of the active compound(s) are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound(s), whereby a formulation with 75% (w/w) of active compound(s) is obtained.
H) Gel-Formulation (GF)
In an agitated ball mill, 20 parts by weight of the active compound(s) are comminuted with addition of 10 parts by weight of dispersants, 1 part by weight of gelling agent wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound(s) suspension. Dilution with water gives a stable suspension of the active compound(s), whereby a formulation with 20% (w/w) of active compound(s) is obtained.
2. Products to be applied undiluted for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.
I) Dustable powders (DP, DS)
5 parts by weight of the active compound(s) are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (w/w) of active compound(s).
J) Granules (GR, FG, GG, MG)
0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound^) is obtained. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.
K) ULV solutions (UL)
10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product having 10% (w/w) of active compound(s), which is applied undiluted for foliar use.
Various types of oils, wetters, adjuvants or bactericides may be added to the active ingredients. Suitable adjuvants in this context are, in particular: organically modified polysiloxanes, e.g. Break Thru S 240™; alcohol alkoxylates, e.g. Atplus 245™, Atplus MBA 1303™, Plurafac LF 300™ and Lutensol ON 30™; EO/PO block polymers, e.g. Pluronic RPE 2035™ and Genapol B™; alcohol ethoxylates, e.g. Lutensol XP 80™; and sodium dioctylsulfosuccinate, e.g. Leophen RA™.
Compositions of this invention may further contain other active ingredients than those listed above. For example further insecticides or fungicides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators and safeners. These agents usually are admixed with the agents according to the invention in a weight ratio of 1 :10 to 10:1.
The pesticidal mixtures may comprise additionally one or more further insecticidal compound III of the following list M of pesticides. The list is intended to illustrate the possible combinations, but not to impose any limitation:
M.1. Organo(thio)phosphates: acephate, azamethiphos, azinphos-ethyl, azinphos- methyl, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos- methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/ DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, flupyrazophos, fosthiazate, heptenophos, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, vamidothion;
M.2. Carbamates: aldicarb, alanycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb, triazamate;
M.3. Pyrethroids: acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-, yfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha- cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, imiprothrin, permethrin, phenothrin, prallethrin, resmethrin, RU 15525, silafluofen, tefluthrin, tetramethrin, tralomethrin, transfluthrin, ZXI 8901 ;
M.4. Juvenile hormone mimics: hydroprene, kinoprene, methoprene, fenoxycarb, pyriproxyfen; M.5. Nicotinic receptor agonists/antagonists compounds: acetamiprid, bensultap, cartap hydrochloride, clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, nicotine, spinosad (allosteric agonist), thiacloprid, thiocyclam, thiosultap- sodium and AKD1022.
M.6. GABA gated chloride channel antagonist compounds: chlordane, endosulfan, gamma-HCH (lindane); acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole, the phenylpyrazole compound of formula M6 1
Figure imgf000059_0001
M.7. Chloride channel activators: abamectin, emamectin benzoate, milbemectin, lepimectin;
M.8. METI I compounds: fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad, flufenerim, rotenone;
M.9. METI Il and III compounds: acequinocyl, fluacyprim, hydramethylnon;
M.10. Uncouplers of oxidative phosphorylation: chlorfenapyr, DNOC;
M.1 1. Inhibitors of oxidative phosphorylation: azocyclotin, cyhexatin, diafenthiuron, fenbutatin oxide, propargite, tetradifon;
M.12. Moulting disruptors: cyromazine, chromafenozide, halofenozide, methoxyfenozide, tebufenozide;
M.13. Synergists: piperonyl butoxide, tribufos;
M.14. Sodium channel blocker compounds: indoxacarb, metaflumizone;
M.15. Fumigants: methyl bromide, chloropicrin sulfuryl fluoride;
M.16. Selective feeding blockers: crylotie, pymetrozine, flonicamid; M.17. Mite growth inhibitors: clofentezine, hexythiazox, etoxazole;
M.18. Chitin synthesis inhibitors: buprofezin, bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron;
M.19. Lipid biosynthesis inhibitors: spirodiclofen, spiromesifen, spirotetramat;
M.20. octapaminergic agonsits: amitraz;
M.21. ryanodine receptor modulators: flubendiamide;
M.22. Various: aluminium phosphide, amidoflumet, benclothiaz, benzoximate, bifenazate, borax, bromopropylate, cyanide, cyenopyrafen, cyflumetofen, chinomethionate, dicofol, fluoroacetate, phosphine, pyridalyl, pyrifluquinazon, sulfur, tartar emetic; pyrimidinyl alkynylether compounds M22 1 or thiadiazolyl alkynylether compounds M222:
Figure imgf000060_0001
wherein RM"22 is methyl or ethyl and Het* is 3,3-dimethylpyrrolidin-1-yl, 3- methylpiperidin-1 -yl, 3,5-dimethylpiperidin-1 -yl, 3-trifluormethylpiperidin-1 -yl, hexahydroazepin-1-yl, 2,6-dimethylhexahydroazepin-1-yl or 2,6-dimethylmorpholin-4-yl.
M.23. N-R'-2,2-dihalo-1-R"cyclo-propanecarboxamide-2-(2,6-dichloro- α,α,α -tri-fluoro- p-tolyl)hydrazone or N-R'-2,2-di(R"')propionamide-2-(2,6-dichloro- α,α,α -trifluoro-p- tolyl)-hydrazone, wherein R' is methyl or ethyl, halo is chloro or bromo, R" is hydrogen or methyl and R'" is methyl or ethyl;
M.24. Anthranilamides: chloranthraniliprole, the compound of formula M24 1
(M24 1)
Figure imgf000060_0002
M.25. Malononitrile compounds: CF3(CH2)2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(CN)2CH2(CF2)5CF2H, CF3(CH2)2C(CN)2(CH2)2C(CF3)2F, CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3, CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(CN)2CH2(CF2)3CF3, CF3(CF2)2CH2C(CN)2CH2(CF2)3CF2H,
CF3CF2CH2C(CN)2CH2(CF2)SCF2H, 2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,4,4,4- pentafluorobutyl)-malonodinitrile, and CF2HCF2CF2CF2CH2C(CN) 2CH2CH2CF2CF3;
M.26. Microbial disruptors: Bacillus thuringiensis subsp. Israelensi, Bacillus sphaericus, Bacillus thuringiensis subsp. Aizawai, Bacillus thuringiensis subsp. Kurstaki, Bacillus thuringiensis subsp. Tenebrionis;
The commercially available compounds of the group M may be found in The Pesticide Manual, 13th Edition, British Crop Protection Council (2003) among other publications.
Thioamides of formula M6 1 and their preparation have been described in WO 98/28279. Lepimectin is known from Agro Project, PJB Publications Ltd, November 2004. Benclothiaz and its preparation have been described in EP-A1 454621. Methidathion and Paraoxon and their preparation have been described in Farm Chemicals Handbook, Volume 88, Meister Publishing Company, 2001. Acetoprole and its preparation have been described in WO 98/28277. Metaflumizone and its preparation have been described in EP-A1 462 456. Flupyrazofos has been described in Pesticide Science 54, 1988, p.237-243 and in US 4822779. Pyrafluprole and its preparation have been described in JP 2002193709 and in WO 01/00614. Pyriprole and its preparation have been described in WO 98/45274 and in US 6335357. Amidoflumet and its preparation have been described in US 6221890 and in JP 21010907. Flufenerim and its preparation have been described in WO 03/007717 and in WO 03/007718. AKD 1022 and its preparation have been described in US 6300348. Chloranthraniliprole has been described in WO 01/70671 , WO 03/015519 and WO 05/118552. Anthranilamide derivatives of formula M24 1 have been described in WO 01/70671 , WO 04/067528 and WO 05/1 18552. Cyflumetofen and its preparation have been described in WO 04/080180. The aminoquinazolinone compound pyrifluquinazon has been described in EP A 109 7932. The alkynylether compounds M22 1 and M222 are described e.g. in JP 2006131529. The malononitrile compounds CF3(CH2)2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(CN)2CH2(CF2)5CF2H, CF3(CH2)2C(CN)2(CH2)2C(CF3)2F, CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3, CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(CN)2CH2(CF2)3CF3, CF3(CF2)2CH2C(CN)2CH2(CF2)3CF2H, CF3CF2CH2C(CN)2CH2(CF2)SCF2H, 2- (2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,4,4,4-pentafluorobutyl)-malonodinitrile, and CF2HCF2CF2CF2CH2C(CN) 2CH2CH2CF2CF3 have been described in WO 05/63694. Those additional ingredients may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a composition of this invention either before or after being treated with other active ingredients.
Applications
The one or more active compound(s) I and the one or more active compound(s) Il can be applied according to different ways of applications, which are I. simultaneously, that is a) jointly (i.e. as mixture as such, e.g. a ready-to-use-formulation, or as tank mix) or b) separately (i.e. application via separate tanks), or
II. in succession separately, the sequence, in this case, generally not having any effect on the result of the control measures.
Therefore, the method for controlling harmful fungi and animal pests is carried out by the separate or joint application of at least one active compound I and at least one of the active compound II, or a mixture of at least one active compounds I and at least one of the active compound II, by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
The inventive mixtures or compositions of these mixtures can also be employed for protecting plants from attack or infestation by insects, acarids or nematodes comprising contacting a plant, or soil or water in which the plant is growing.
In the context of the present invention, the term plant refers to an entire plant, a part of the plant or the propagation material of the plant, that is, the seed or the seedling.
Plants which can be treated with the inventive mixtures include all genetically modified plants or transgenic plants, e.g. crops which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods, or plants which have modified characteristics in comparison with existing plants, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures.
Some of the inventive mixtures have systemic action and can therefore be used for the protection of the plant shoot against foliar pests as well as for the treatment of the seed and roots against soil pests.
The mixtures of compounds I and Il or their corresponding formulations are applied by treating the harmful fungi and the animal pests, their habitat or the plants, seeds, soils, areas, materials or spaces to be kept free from them with a pesticidally effective amount of the mixture or, in the case of separate application, of the compounds I and II. Application can be before or after the infection by harmful fungi and/or animal pests.
In general, "pesticidally effective amount" means the amount of the inventive mixtures or of compositions comprising the mixtures needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various mixtures / compositions used in the invention. A pesticidally effective amount of the mixtures / compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.
Preferred application methods are into water bodies, via soil, cracks and crevices, pastures, manure piles, sewers, into water, on floor, wall, or by perimeter spray application and bait.
Usually, mixtures of at least one compound I and at least one active compound Il are employed. However, mixtures of at least one compound I with two or, if desired, more active components may also offer particular advantages.
Suitable further active components in the above sense are particularly the active compounds Il mentioned at the outset and in particular the preferred active compounds Il mentioned above.
The inventive mixtures and the compositions comprising them can be used for protecting wooden materials such as trees, board fences, sleepers, etc. and buildings such as houses, outhouses, factories, but also construction materials, furniture, leathers, fibers, vinyl articles, electric wires and cables etc. from ants and/or termites, and for controlling ants and termites from doing harm to crops or human being (e.g. when the pests invade into houses and public facilities).
In the case of soil treatment or of application to the pests dwelling place or nest, the quantity of active ingredient(s) ranges from 0.0001 to 500 g per 100 m2, preferably from 0.001 to 2O g per 100 m2.
Customary application rates in the protection of materials are, for example, from 0.01 g to 1000 g of active compound(s) per m2 treated material, desirably from 0.1 g to 50 g per m2. Pesticidal compositions for use in the impregnation of materials typically contain from 0.001 to 95 weight %, preferably from 0.1 to 45 weight %, and more preferably from 1 to 25 weight % of at least one repellent and / or insecticide.
For use in spray compositions, the content of the mixture of the active ingredients is from 0.001 to 80 weights %, preferably from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight %.
In general, "synergistically effective amount" means that the one or more active compound(s) I and the one or more active compound(s) Il are usually applied in a weight ratio of from 500:1 to 1 :100, preferably from 20:1 to 1 :50, in particular from 5:1 to 1 :20. Depending on the nature of the compounds the employed weight ratio of compound(s) I and compound(s) Il ranges can start from 100:1 to 1 :100, preferably from 20:1 to 1 :20, in particular from 10:1 to 1 :10.
Further active copmpounds are, if desired, mixed in a ratio of from 20:1 to 1 :20 to the compound I.
Depending on the desired effect, the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 20 to 1500 g/ha, more preferably from 50 to 1000 g/ha and in particular from 50 to 750 g/ha. For use in treating crop plants, the rate of application of the mixture of the active ingredients of this invention may be in the range of 0.1 g to 4000 g per hectare, desirably from 25 g to 600 g per hectare, more desirably from 50 g to 500 g per hectare.
Correspondingly, the application rates for the compound(s) I are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
Correspondingly, the application rates for the active compound Il are generally from 1 to 2000 g/ha, preferably from 10 to 1500 g/ha, in particular from 40 to 1000 g/ha.
Methods to control infectious diseases transmitted by insects (e.g. malaria, dengue and yellow fever, lymphatic filariasis, and leishmaniasis) with the inventive mixtures and their respective compositions also comprise treating surfaces of huts and houses, air spraying and impregnation of curtains, tents, clothing items, bed nets, tsetse-fly trap or the like, lnsecticidal compositions for application to fibers, fabric, knitgoods, non- wovens, netting material or foils and tarpaulins preferably comprise a composition including the inventive mixtures, optionally a repellent and at least one binder.
Bait formulations and applications The mixtures according to the invention can be applied to any and all developmental stages, such as egg, larva, pupa, and adult. The pests may be controlled by contacting the target pest, its food supply, habitat, breeding ground or its locus with a pesticidally effective amount of the inventive mixtures or of compositions comprising the mixtures.
"Locus" in general means a plant, seed, soil, area, material or environment in which pests or fungi are growing or may grow.
The mixtures according to the invention are effective through both contact and ingestion.
The inventive mixtures are effective through both contact (via soil, glass, wall, bed net, carpet, plant parts or animal parts), and ingestion (bait, or plant part) and through trophallaxis and transfer.
According to another preferred embodiment of the invention, for use against non crop pests such as ants, termites, wasps, flies, mosquitoes, crickets, locusts, or cockroaches the inventive mixtures are prepared into a bait preparation.
The bait can be a liquid, a solid or a semisolid preparation (e.g. a gel). The bait employed in the composition is a product which is sufficiently attractive to incite insects such as ants, termites, wasps, flies, mosquitoes, crickets etc. or cockroaches to eat it. This attractant may be chosen from feeding stimulants or para and / or sex pheromones readily known in the art.
For use in bait compositions, the typical content of active ingredient(s) is from 0.0001 weight % to 15 weight %, desirably from 0.001 weight % to 5% weight % of active compound. The composition used may also comprise other additives such as a solvent of the active material, a flavoring agent, a preserving agent, a dye or a bitter agent. Its attractiveness may also be enhanced by a special color, shape or texture.
According to a preferred embodiment of the invention, the mixtures according to the present invention are employed via soil application. Soil application is especially favorable for use against ants, termites, crickets, or cockroaches.
According to another preferred embodiment of the invention, for use against non crop pests such as ants, termites, wasps, flies, mosquitoes, crickets, locusts, or cockroaches the mixtures according to the present invention are prepared into a bait preparation. Seed Treatment
The mixtures according to the present invention are also suitable for the treatment of seeds in order to protect the seed from harmful fungi and animal pests, in particular from soil-living fungi and insect pests and the resulting plant's roots and shoots against soil pests and foliar insects. The protection of the resulting plant's roots and shoots is preferred.
The present invention therefore comprises therefore a method for the protection of seeds from insects, in particular from soil pests and of the seedlings' roots and shoots from harmfulo fungi and insects, in particular from soil and foliar insects, said method comprising contacting the seeds before sowing and/or after pregermination with mixtures according to the present invention.
Particularly preferred is a method, wherein the plant's roots and shoots are protected.
The term seed embraces seeds and plant propagules of all kinds including but not limited to true seeds, seed pieces, suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots and the like and means in a preferred embodiment true seeds.
The term seed treatment comprises all suitable seed treatment techniques known in the art, such as seed dressing, seed coating, seed dusting, seed soaking and seed pelleting.
The present invention also comprises seeds coated with or containing the active compounds. The term "coated with and/or containing" generally signifies that the active ingredients are for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product are (re)planted, it may absorb the active ingredient.
Suitable seeds are seeds of cereals, root crops, oil crops, vegetables, spices, ornamentals, for example seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geranium/pelargoniums, pansies and impatiens.
In addition, the mixtures according to the invention may also be used for the treatment seeds from plants, which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods.
For example, the active mixtures can be employed in treatment of seeds from plants, which are resistant to herbicides from the group consisting of the sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogous active substances (see for example, EP-A-0242236, EP-A-242246) (WO 92/00377) (EP-A-0257993, U.S. Pat. No. 5,013,659) or in transgenic crop plants, for example cotton, with the capability of producing Bacillus thuringiensis toxins (Bt toxins) which make the plants resistant to certain pests (EP-A-0142924, E P-A-0193259),
Furthermore, the mixtures according to the present invention can be used also for the treatment of seeds from plants, which have modified characteristics in comparison with existing plants consist, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures). For example, a number of cases have been described of recombinant modifications of crop plants for the purpose of modifying the starch synthesized in the plants (e.g. WO 92/11376, WO 92/14827, WO 91/19806) or of transgenic crop plants having a modified fatty acid composition (WO 91/13972).
The seed treatment application of the mixtures is carried out by spraying or by dusting the seeds before sowing of the plants and before emergence of the plants.
In the treatment of seeds the corresponding formulations are applied by treating the seeds with an effective amount of the mixture according to the present invention. Herein, the application rates of the active compound(s) are generally from 0,1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 2,5 kg per 100 kg of seed. For specific crops such as lettuce the rate can be higher.
Compositions, which are especially useful for seed treatment are e.g.:
A Soluble concentrates (SL, LS)
D Emulsions (EW, EO, ES)
E Suspensions (SC, OD, FS) F Water-dispersible granules and water-soluble granules (WG, SG)
G Water-dispersible powders and water-soluble powders (WP, SP, WS)
H Gel-Formulations (GF)
I Dustable powders (DP, DS)
Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulations can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds or after having pregerminated the latter
In a preferred embodiment a FS formulation is used for seed treatment. Typcially, a FS formulation may comprise 1-800 g/l of active ingredient(s), 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.
Preferred FS formulations of the active compounds for seed treatment usually comprise from 0.1 to 80% by weight (1 to 800 g/l) of the active ingredient(s), from 0.1 to 20 % by weight (1 to 200 g/l) of at least one surfactant, e.g. 0.05 to 5 % by weight of a wetter and from 0.5 to 15 % by weight of a dispersing agent, up to 20 % by weight, e.g. from 5 to 20 % of an anti-freeze agent, from 0 to 15 % by weight, e.g. 1 to 15 % by weight of a pigment and/or a dye, from 0 to 40 % by weight, e.g. 1 to 40 % by weight of a binder (sticker /adhesion agent), optionally up to 5 % by weight, e.g. from 0.1 to 5 % by weight of a thickener, optionally from 0.1 to 2 % of an anti-foam agent, and optionally a preservative such as a biocide, antioxidant or the like, e.g. in an amount from 0.01 to 1 % by weight and a filler/vehicle up to 100 % by weight.
Seed Treatment formulations may additionally also comprise binders and optionally colorants.
Binders can be added to improve the adhesion of the active materials on the seeds after treatment. Suitable binders are block copolymers EO/PO surfactants but also polyvinylalcoholsl, polyvinylpyrrolidones, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyleneimines (Lupasol®, Polymin®), polyethers, polyurethans, polyvinylacetate, tylose and copolymers derived from these polymers.
Optionally, also colorants can be included in the formulation. Suitable colorants or dyes for seed treatment formulations are Rhodamin B, C.I. Pigment Red 112, C.I. Solvent Red 1 , pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108. The invention also relates to seed comprising mixtures according to the present invention. The amount of the compound I or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, more preferably from 1 g to 1000 g per 100 kg of seeds, most preferably from 1 g to 750 g per 100 kg of seeds, and in particular from 5 g to 500 g per 100 kg of seed.
Biology
B.1 Fungicidal action
The fungicidal effect of the compound and the mixtures can be demonstrated by the following tests:
The active compounds, separately or jointly, are prepared as a stock solution comprising 0.25% by weight of active compounds in acetone or DMSO. 1 % by weight of the emulsifier Uniperol® EL (wetting agent having emulsifying and dispersant action based on ethoxylated alkylphenols) is added to this solution, and the mixture is diluted with water to the desired concentration.
The visually determined percentages of infected leaf areas are converted into efficacies in % of the untreated control:
The efficacy (E) is calculated as follows using Abbot's formula:
E = (1 - α/β ) ■ 100
α corresponds to the fungicidal infection of the treated plants in % and β corresponds to the fungicidal infection of the untreated (control) plants in %
An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants are not infected.
The expected efficacies of mixtures of active compounds is determined using Colby's formula (Colby, S. R. "Calculating synergistic and antagonistic responses of herbicide Combinations", Weeds, ^5, 20-22, 1967) and compared with the observed efficacies.
Colby's formula: E = x + y - x-y/100 E expected efficacy, expressed in % of the untreated control, when using the mixture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active compound A at the concentration a y efficacy, expressed in % of the untreated control, when using the active compound B at the concentration b
Example B.1a Fungicidal control of brown spot caused by Cochliobolus miyabeanus
(protective)
Leaves of pot-grown rice seedlings are sprayed to run-off with an aqueous suspension containing a certain concentration of active ingredients prepared from a stock solution.
The plants are allowed to air-dry. At the following day the plants are inoculated with an aqueous spore suspension of Cochliobolus miyabeanus. Then the trial plants are immediately transferred to a humid chamber. After 6 days at 22-24O and a relative humidity close to 100 % the extent of fungal attack on the leaves is visually assessed as
% diseased leaf area.
B.2. Action against animal pests
The following tests can demonstrate the control efficacy of compounds, mixtures or compositions of this invention on specific pests. However, the pest control protection afforded by the mixtures is not limited to these species. In certain instances, combinations of a compound of this invention with other invertebrate pest control compounds or agents are found to exhibit synergistic effects against certain important invertebrate pests.
The analysis of synergism of the mixtures is determined using Colby's equation.
Example B.2a lnsecticidal control of vetch aphid (Megoura viciae)
For evaluating control of vetch aphid (Megoura viciae) through contact or systemic means the test unit consists of 24-well-microtiter plates containing broad bean leaf disks. The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
DMSO. Different concentrations of formulated mixtures are sprayed onto the leaf disks at 2.5μl, using a custom built micro atomizer at two replications.
For experimental mixtures in these tests identical volumes of both mixing partners at the desired concentrations respectively are mixed together. After application, the leaf disks are air-dried and 5 - 8 adult aphids placed on the leaf disks inside the microtiter plate wells. The aphids are then allowed to suck on the treated leaf disks and are incubated at 23 + 10C, 50 + 5 % room humidity for 5 days. Aphid mortality and fecundity is then visually assessed.
Example B.2b lnsecticidal control of boll weevil (Anthonomus grandis)
For evaluating control of boll weevil (Anthonomus grandis) the test unit consists of 24- well-microtiter plates containing an insect diet and 20-30 A. grandis eggs.
The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
DMSO. Different concentrations of formulated mixtures are sprayed onto the insect diet at 20μl, using a custom built micro atomizer at two replications.
For experimental mixtures in these tests identical volumes of both mixing partners at the desired concentrations respectively are mixed together.
After application the microtiter plates are incubated at 23 + 10C, 50 +_ 5 % room humidity for 5 days. Egg and larval mortality is then visually assessed.
Example B.2c lnsecticidal control of Mediterranean fruitfly (Ceratitis capitata)
For evaluating control of Mediterranean fruitfly (Ceratitis capitata) the test unit consists of 96-well-microtiter plates containing an insect diet and 50-80 C. capitata eggs. The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
DMSO. Different concentrations of formulated mixtures are sprayed onto the insect diet at 5μl, using a custom built micro atomizer at two replications.
For experimental mixtures in these tests identical volumes of both mixing partners at the desired concentrations respectively, are mixed together. After application, microtiter plates are incubated at 28 +_ 10C, 80 + 5 % room humidity for 5 days. Egg and larval mortality is then visually assessed.
Example B.2d lnsecticidal control of tobacco budworm (Heliothis virescens)
For evaluating control of tobacco budworm (Heliothis virescens) the test unit consists of
96-well-microtiter plates containing an insect diet and 15-25 H. virescens eggs.
The mixtures are formulated using a solution containing 75 wt% water and 25 wt%
DMSO. Different concentrations of formulated mixtures are sprayed onto the insect diet at 10μl, using a custom built micro atomizer at two replications. For experimental mixtures in these tests identical volumes of both mixing partners at the desired concentrations respectively are mixed together.
After application, microtiter plates were incubated at 28 + 10C, 80 + 5 % room humidity for 5 days. Egg and larval mortality was then visually assessed.
Synergism is demonstrated, when the activity of the mixtures according to the invention is considerably higher than predicted using Colby's formula. Following compounds C of the invention were tested with different products (as mixing partners) as listed below:
Compound C.1.5 Compound C.1.10
Figure imgf000072_0001
Compound C.1.2
Figure imgf000072_0002
Mixing product: benthiavalicarb, cymoxanil, dithianon, epoxiconazol, fluxastrobin, picoxystrobin, quinoxyfen and tebuconazol
The active compounds were formulated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide. The stock solutions were mixed according to the given ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of the pathogen to be treated was then added and after 7 days of inoculation, the MTP was measured using an absorption photometer. The measured parameters were compared to the growth of the active compound-free control variant (100%) and the fungus-free and active compound-free blank value to determine the relative growth in % of the pathogens in the respective active compounds. The visually determined percentages of infected leaf areas were converted into efficacies in % of the untreated control.
Test 1. Activity against the grey mold Botrytis cinerea in the microtiterplate test (Botrci) The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Botrci cinerea in an aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 1
Table 1 : Botrci
Figure imgf000073_0001
2. Activity against the late blight pathogen Phytophthora infestans in the microtiter test (Phytin)
The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Phytophtora infestans containing a pea juice-based aqueous nutrient medium was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 2
Table 2: Phytin
Figure imgf000074_0001
3. Activity against rice blast Pyricularia oryzae in the microtiterplate test (Pyrior)
The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Pyricularia oryzae in an aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 3 Table 3: Pyrior
Figure imgf000075_0001
4. Activity against leaf blotch on wheat caused by Septoria tritici (Septtr)
The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Septoria tritici in an aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The results for the tested mixtures are listed in table 4
Table 4: Septtr
Figure imgf000076_0001

Claims

Claims
1. A pesticidal mixture comprising at least two active compounds, wherein:
1 ) at least one active compound I is a cyanosulfoximine compound of the formula (I)
Figure imgf000077_0001
formula (I)
wherein
is selected from
Figure imgf000077_0002
and wherein # denotes the bonding in formula I;
R1 is Cl or CF3 and
R2 is selected from hydrogen, chloro, CH3 or C2H5;
or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers
and
2) at least one active compound Il is a fungicidal compound selected from the groups I LA to 11. F:
11. A azoles such as triazoles, imidazoles, pyrazoles, thiazoles and oxa- zoles selected from the group consisting of azaconazole, benomyl, bitertanol, bromuconazole, carbendazim, cyproconazole, cyazofamid, difenoconazole, diniconazole, diniconazole-M, enilconazole, epoxi- conazole, ethaboxam, etridiazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, fuberidazole, hexaconazole, hymexazole, ima- zalil, imazalil-sulfphate, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazol, paclobutrazol, pefurazoate, penconazole, prochloraz, propiconazole, prothioconazole, simeconazole, triadime- fon, triadimenol, tebuconazole, tetraconazole, thiabendazole, triti— conazole, triflumizole, uniconazol, 1-(4-chloro-phenyl)-2- ([1 ,2,4]triazol-1 -yl)-cycloheptanol;
II. B strobilurins selected from the group consisting of azoxystrobin, di- moxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, methomi- nostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyribencarb, tri- floxystrobin, methyl 2-(ortho-(2,5- dimethylphenyloxymethylene)phenyl)-3-methoxy-acrylate, 2-(2-(6-(3- chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2- methoxyimino-N-methyl-acetamide and 3-methoxy-2-(2-(N-(4- methoxy-pheny^-cyclo-propanecarboximidoylsulfanylmethy^-phenyl)- acrylic acid methyl ester;
11. C carboxamides selected from the group consisting of benalaxyl, benalaxyl-M, benodanil, bixafen, boscalid, car- boxin, carpropamid, dimethomorph, diclocymet, fen- hexamid, fluopyram, flutolanil, furametpyr, flumorph, flu- metover, fluopicolide (picobenzamid), isopyrazam, mandipropamid, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, oxytetracyclin, pen- thiopyrad, silthiofam,thifluzamide, tiadinil, zoxamide, 5-fluoro-1 ,3-dimethyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,2-dimethyl- propyl)-phenyl]-amide, methyl-3-(4-chlorophenyl)-
3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)propionate, 2- chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide, N-(3-ethyl-3,5-5- trimethyl-cyclohexyl)-3-formylamino-2-hydroxy-benzamide, N-(2-{4-[3- (4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4- chlorophenyl)-prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- ethanesulfonylamino-3-methyl-butyramide, N-(6-methoxy-pyridin-3-yl) cyclopropane-carboxamide, 2-amino-4-methyl-thiazole-5- carboxamide, N-(2-cyanophenyl)-3,4-dichloroisothiazole-5- carboxamide, N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4- difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-chloro-3'- fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4- difluoromethyl-2-methylthiazole-5-carboxamide, N-(3',4'-dichloro-4- fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4- carboxamide, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl- 1-methylpyrazole-4-carboxamide; N-(3',4'-dichloro-4-fluorobiphenyl-2- yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide, N-(3\4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl- 1 -methylpyrazole-4-carboxamide, N-(2-(1 ,3-dimethylbutyl)-phenyl)-
1 ,3-dimethyl-5-fluoro-1 H-pyrazole-4-carboxamide, N-(4'-chloro-3',5- difluoro-biphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carbox amide, N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3- trifluoromethyl-1-methyl-1 H-pyrazole-4-carbox amide, N-(3',4'- dichloro-5-fluoro-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl-1 H- pyrazole-4-carbox amide, N-(3',5-difluoro-4'-methyl-biphenyl-2-yl)-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-ca rboxamide,N-(3', 5-d ifluoro- 4'-methyl-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-(trans-2-bicyclopropyl-2-yl- phenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N- (2',4'-difluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole- 4- carboxamide, N-(2',4'-dichlorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',4'-difluorobiphenyl- 2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(2',4'- dichlorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2',5'-difluorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-(2',5'-dichlorobiphenyl- 2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',5'- difluorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2',5'-dichlorobiphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole- 4-carboxamide, N-(3',5'-difluorobiphenyl-2-yl)-1- methyl-3-trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-(3',5'- dichlorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole- 4- carboxamide, N-(3',5'-difluorobiphenyl-2-yl)-3-difluoromethyl-1 - methyl-1 H-pyrazole- 4-carboxamide, N-(3',5'-dichlorobiphenyl-2-yl)-3- difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(3'- fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3'-chlorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl- 1 H-pyrazole-4-carboxamide; N-(3'-fluorobiphenyl-2-yl)-3- difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(3'- chlorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(2'-fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H- pyrazole-4-carboxamide, N-(2'-chlorobiphenyl-2-yl)-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(2'-fluorobiphenyl-2-yl)-
3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-(2'- chlorbiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide; N-(2'-fluoro-4'-chloro-5'-methylbiphenyl-2-yl)-1 -methyl- 3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4',5'- trifluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-1 -methyl-3- difluoromethyl-1 H-pyrazole-4-carboxamide, N-(2',4',5'- trifluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-chlorofluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-[2-(1 ,1 ,2,3,3,3- hexafluoropropoxy)phenyl]-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-[2-(1 ,1 , 2,3,3, 3-hexafluoropropoxy)-phenyl]-3- difluoromethyl-1-methyl-1 H-pyrazole-4-carboxamide, N-[2-(2-chloro-
1 ,1 ,2-trifluoroethoxy)phenyl]-1-methyl-3-trifluoromethyl-1 H-pyrazole- 4-carboxamide, N-[2-(2-chlor-1 ,1 ,2-trifluoroethoxy)phenyl]- 3- difluoromethyl-1-methyl-1 H-pyrazole-4-carboxamide, N-[2-(1 ,1 ,2,2- tetrafluoroethoxy)phenyl]-3-difluoromethyl-1-methyl-1 H-pyrazole-4- carboxamide, N-[2-(1 , 1 ,2,2-tetrafluoroethoxy)phenyl]-1 -methyl-3- trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'- (trifluoromethylthio)biphenyl-2-yl)-3-difluoromethyl-1-methyl-1 H- pyrazole-4-carboxamide, N-(4'-(trifluoromethylthio)biphenyl-2-yl)-1- methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide;
11. D heterocyclic compounds selected from the group consisting of aci- benzolar-S-methyl, anilazine, aldimorph, blasticidin-S, bupirimate, captafol, captan, chinomethionat, cyprodinil, dazomet, debacarb, di- clomezine, difenzoquat, difenzoquat-methylsulphat, diflumetorim, do- demorph, dodemorph-acetate, famoxadone, fenamidone, fenarimol, ferimzone, fenpiclonil, fenpropidin, fenpropimorph, fludioxonil, fluazi- nam, fluoroimid, flutianil, folpet, fenoxanil, iprodione, mepanipyrim, ni- trapyrin, nuarimol, octhilinone, oxolinic acid, piperalin, probenazole, procymidone, proquinazid, pyrifenox, pyrimethanil, pyroquilon, qui- noxyfen, tricyclazole, triforine, tridemorph, vinclozolin, 5-chloro-7-(4- methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5- a]pyrimidine, 6-(4-tert-butylphenyl)-5-methyl-[1 ,2,4]triazolo[1 ,5- a]pyrimidine-7-ylamine, 5-methyl-6-(3,5,5-trimethyl-hexyl)- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-ylamine, 5-methyl-6-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 6-methyl-5-octyl-
[1 ,2,4]tri-azolo[1 ,5-a]pyrimidine-7-yl-amine, 6-ethyl-5-octyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 5-ethyl-6-octyl- [1 ,2,4]triazolo[1 ,5-a]pyri-midine-7-ylamine, 5-ethyl-6-(3,5,5-trimethyl- hexyl)-[1 ,2,4]tri-azo-lo[1 ,5-a]pyrimi-dine-7-ylamine, 6-octyl-5-propyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 5-methoxy-methyl-6-octyl-
[1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine, 6-octyl-5-trifluoromethyl- [1 ,2,4]triazolo[1 ,5-a]pyrimidine-7-yl-amine and 5-trifluoromethyl-6- (3,5,5-trimethyl-hexyl)-[1 ,2,4]tri-azolo[1 ,5-a]pyrimidine-7-ylamine, 2,3,5,6-tetrachloro-4-methanesulfonyl-pyridine, 3,4,5-trichloro- pyridine-2,6-di-carbonitrile, N-(1-(5-bromo-3-chloro-pyridin-2-yl)- ethyl)-2,4-dichloro-nicotinamide, N-((5-bromo-3-chloro-pyridin-2-yl)- methyl)-2,4-dichloro-nicotinamide, 2-butoxy-6-iodo-3-propylchromen- 4-one and N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1- sulfonyl)-[1 ,2,4]triazole-1 -sulfonamide;
carbamates selected from the group consisting of diethofencarb, fer- bam, flubenthiavalicarb, iprovalicarb, mancozeb, maneb, metam, methasulphocarb, metiram, propamocarb, propamocarb hydrochlo- rid,propineb, thiram, zineb, ziram, 4-fluorophenyl N-(1-(1-(4- cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, methyl 3-(4- chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate and carbamate oxime ethers of the formula
| |E 1
Figure imgf000081_0001
Z = N7 CH
fungicides selected from the group of antibiotics comprising kasugamycin, kasugamycin- hydrochlorid-hydrat , mildiomycin, streptomycin, polyoxin and valida- mycin A; the group of nitrophenyl derivatives comprising binapacryl, dinocap, dinobuton, dicloran, nitrothal-isopropyl and tecnazen; the group of sulfur-containing heterocyclyl compounds comprising di- thianon and isoprothiolane; the group of organometallic compounds comprising fentin salts; the group of organophosphorus compounds comprising edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos and tolclofos-methyl; the group of organochlorine compounds comprising chlorothalonil, di- chlofluanid, dichlorophen, pentachlorophenol and its salts, flusul- famide, hexachlorobenzene, phthalide, pencycuron, quintozene, thio- phanate-methyl and tolylfluanid; the group of inorganic active compounds comprising Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, oxin-copper and sulfur; and/or selected from a group of various fungicides consisting of bi- phenyl, bronopol, cyflufenamid, cymoxanil, diphenylamine, dimethiri- mol, dodine, dodine free base, ethirimol, furalaxyl, iminoctadine, imi- noctadine-triacetate, iminoctadine-tris(albesilate), guazatine, guaza- tine-acetate, metrafenone, prohexadione calcium, spiroxamine gua- nidine, N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl-benzenesulfon- amide, N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3-difluoro- phenyl)-methyl)-2-phenyl acetamide, N'-(4-(4-chloro-3-trifluoromethyl- phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'-(4- (4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N- methyl formamidine, N'-(2-methyl-5-trifluormethyl-4-(3- trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine and N'-(5-difluormethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N- ethyl-N-methyl formamidine;
in a synergistically effective amount.
2. The pesticidal mixture according to claim 1 comprising additionally one or more further insecticidal compound III.
3. Pesticidal mixtures according to claim 1 or 2, wherein the substituents of the compound I of formula (I) have the following meanings:
R1 is CF3 or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers.
4. Pesticidal mixtures according to claim 1 or 2, wherein the substituents of the compound I of formula (I) have the following meanings:
R1 is Cl or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers.
5. Pesticidal mixtures according to claim 1 or 2, wherein the substituents of the compound I of formula (I) have the following meanings: G is G1 and
R2 is CH3 or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers.
6. Pesticidal mixtures according to claim 1 or 2, wherein the substituents of the compound I of formula (I) have the following meanings:
G is G2 and
R2 is hydrogen or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers.
7. Pesticidal mixtures according to claim 1 or 2, wherein the substituents of the active compound I of formula I have the following meanings:
G is G1 and R2 is hydrogen, chloro or C2H5; or an enantiomer or a diastereomer thereof, pure or as mixtures of these enanti- omers and/or diastereomers.
8. The pesticidal mixture according to claim 1 or 2, comprising a compound I of the formula (I) and a compound Il in a weight ratio of from 100:1 to 1 :100.
9. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il selected from the group 11. A of azoles constisting of benomyl, carbendazim, epoxiconazole, fluquinconazole, flutriafol, flusilazole, metconazole, prochloraz, prothioconazole, tebuconazole and triticonazole.
10. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il is the strobilurin pyracolstrobin.
1 1. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il selected from the group II. C of carboxamides consisting of boscalid, dimetho- morph and penthiopyrad.
12. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il selected from the group II. D of heterocyclic compounds consisiting of dode- morph, famoxadone, fenpropimorph, proquinazid pyrimethanil, tridemorph and 5- chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5- a]pyrimidine.
13. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il selected from the group 11. E of carbamates consisiting of maneb, mancozeb, metiram and thiram.
14. The pesticidal mixture according to claim 1 or 2, comprising an active compound Il selected from the group 11. F of other fungicides consisting of chlorothalonil, di- thianon, flusulfamide,metrafenone and phosphorous acid and its salts.
15. A ternary or quaternary pesticidal mixture according to claim 1 or 2, comprising two active compounds II.
16. A pesticidal composition, comprising a liquid or solid carrier and a mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15.
17. A method for controlling phytopathogenic harmful fungi, wherein the fungi, their habitat or the plants to be protected against fungal attack, the soil or seed are treated with an effective amount of a mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15.
18. A method for protecting plants from phytopathogenic harmful fungi, wherein the fungi, their habitat or the plants to be protected against fungal attack, the soil or seed are treated with an effective amount of a mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15.
19. A method for controlling insects, arachnids or nematodes comprising contacting an insect, acarid or nematode or their food supply, habitat, breeding grounds or their locus with an effective amount of a mixture of at least one active compound
I and at least one active compound Il according to any of claims 1 to 15.
20. A method for protecting plants from attack or infestation by insects, acarids or nematodes comprising contacting the plant, or the soil or water in which the plant is growing with an effective amount of a mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15.
21. A method according to claims 17 to 20, wherein the mixture as claimed in claims 1 to 15 is applied in an amount of from 5 g/ha to 2000 g/ha.
22. A method for protection of seed comprising contacting the seeds with an effective amount of a mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15.
23. A method according to claim 22 wherein the mixture of the active compound I and the active compound Il according to any of claims 1 to 15 is applied in an amount of from 0.001 g to 10 kg per 100 kg of seeds.
24. Seed, comprising the mixture of at least one active compound I and at least one active compound Il according to any of claims 1 to 15 in an amount of from 0.1 g to 10 kg per 100 kg of seeds.
25. A method according to claims 17 to 20 or 22, wherein the active compound I and the active compound Il as defined in any of claims 1 to 15 are applied simultaneously, that is jointly or separately, or in succession.
26. Use of a mixture as defined in claims 1 to 15 for combating insects, arachnids or nematodes.
27. Use of a mixture as defined in claims 1 to 15 for combating phytopathogenic harmful fungi.
PCT/EP2008/065213 2007-11-16 2008-11-10 Pesticidal mixtures comprising cyanosulfoximine compounds Ceased WO2009062905A1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
JP2010533550A JP2011503138A (en) 2007-11-16 2008-11-10 Pesticide mixture containing cyanosulfoximine compound
BRPI0819823A BRPI0819823B1 (en) 2007-11-16 2008-11-10 pesticide mixture, pesticide composition, methods for controlling harmful phytopathogenic fungi, for protecting plants from harmful phytopathogenic fungi and for seed protection, and use of a mixture
BR122018016271-6A BR122018016271B1 (en) 2007-11-16 2008-11-10 PESTICIDE MIXTURE, PESTICIDE COMPOSITION, METHODS TO CONTROL HARMFUL PHYTOPATOGENIC FUNGI, TO PROTECT PLANTS FROM HARMFUL PHYTOPATOGENIC FUNGI AND FOR SEED PROTECTION, AND, USE OF A MIXTURE
ES08851006.0T ES2554768T3 (en) 2007-11-16 2008-11-10 Pesticide mixtures comprising cyanosulfoximin compounds
US12/742,766 US20110105321A1 (en) 2007-11-16 2008-11-10 Pesticidal Mixtures Comprising Cyanosulfoximine Compounds
BR122018004457-8A BR122018004457B1 (en) 2007-11-16 2008-11-10 PESTICIDE MIXTURE, PESTICIDE COMPOSITION, METHODS FOR CONTROLLING HARMFUL PHYTOPATHOGENIC FUNGES, PROTECTION OF PLANTS, AND FOR PROTECTION OF SEED AND, USE OF A MIXTURE
CN200880124587XA CN101909448A (en) 2007-11-16 2008-11-10 Pesticide mixtures containing cyanosulfoximine compounds
PL08851006T PL2219456T3 (en) 2007-11-16 2008-11-10 Pesticidal mixtures comprising cyanosulfoximine compounds
EP08851006.0A EP2219456B1 (en) 2007-11-16 2008-11-10 Pesticidal mixtures comprising cyanosulfoximine compounds
IL205622A IL205622A0 (en) 2007-11-16 2010-05-09 Pesticidal mixtures comprising cyanosulfoximine compounds
US14/136,863 US20140179518A1 (en) 2007-11-16 2013-12-20 Pesticidal Mixtures Comprising Cyanosulfoximine Compounds

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US98861807P 2007-11-16 2007-11-16
US60/988,618 2007-11-16

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/742,766 A-371-Of-International US20110105321A1 (en) 2007-11-16 2008-11-10 Pesticidal Mixtures Comprising Cyanosulfoximine Compounds
US14/136,863 Continuation US20140179518A1 (en) 2007-11-16 2013-12-20 Pesticidal Mixtures Comprising Cyanosulfoximine Compounds

Publications (1)

Publication Number Publication Date
WO2009062905A1 true WO2009062905A1 (en) 2009-05-22

Family

ID=40329175

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2008/065213 Ceased WO2009062905A1 (en) 2007-11-16 2008-11-10 Pesticidal mixtures comprising cyanosulfoximine compounds

Country Status (10)

Country Link
US (2) US20110105321A1 (en)
EP (1) EP2219456B1 (en)
JP (1) JP2011503138A (en)
KR (1) KR101605569B1 (en)
CN (1) CN101909448A (en)
BR (3) BRPI0819823B1 (en)
ES (1) ES2554768T3 (en)
IL (1) IL205622A0 (en)
PL (1) PL2219456T3 (en)
WO (1) WO2009062905A1 (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010040623A1 (en) * 2008-10-08 2010-04-15 Syngenta Participations Ag Pesticidal combinations containing sulfoxaflor
WO2010074751A1 (en) * 2008-12-26 2010-07-01 Dow Agrosciences, Llc Stable sulfoximine-insecticide compositions
WO2010023171A3 (en) * 2008-08-28 2010-12-23 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds and spinetoram
JP2011246459A (en) * 2010-04-28 2011-12-08 Sumitomo Chemical Co Ltd Pesticidal composition and use thereof
WO2012000946A2 (en) 2010-06-30 2012-01-05 Bayer Cropscience Ag Active ingredient combinations
JP2012102077A (en) * 2010-10-14 2012-05-31 Sumitomo Chemical Co Ltd Noxious organism-preventing/eliminating composition and noxious organism-preventing/eliminating method
EP2481284A3 (en) * 2011-01-27 2012-10-17 Basf Se Pesticidal mixtures
US8507532B2 (en) 2008-12-26 2013-08-13 Dow Agrosciences, Llc. Stable insecticide compositions and methods for producing same
US9161539B2 (en) 2010-04-28 2015-10-20 Sumitomo Chemical Company, Limited Plant disease control composition and its use
US9232797B2 (en) 2010-04-27 2016-01-12 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9232798B2 (en) 2010-04-27 2016-01-12 Sumitomo Chemical Company, Limited Pesticidal composition and its use
AU2014256417B2 (en) * 2008-12-26 2016-04-14 Corteva Agriscience Llc Stable sulfoximine-insecticide compositions
US9363998B2 (en) 2010-04-28 2016-06-14 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9375003B2 (en) 2010-04-28 2016-06-28 Sumitomo Chemical Company, Limited Plant disease control composition and its use
US9888685B2 (en) 2007-04-12 2018-02-13 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2363023A1 (en) * 2010-03-04 2011-09-07 Basf Se Synergistic fungicidal and insecticidal mixtures
JP5776293B2 (en) * 2011-04-15 2015-09-09 住友化学株式会社 Harmful arthropod control composition and harmful arthropod control method
JP5776294B2 (en) * 2011-04-15 2015-09-09 住友化学株式会社 Harmful arthropod control composition and harmful arthropod control method
RU2592515C2 (en) * 2011-06-07 2016-07-20 ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи Oil dispersion of sulfoxymines for pest control
CN104397010A (en) * 2014-11-26 2015-03-11 广东中迅农科股份有限公司 Tefluthrin and sulfoxaflor containing pesticide composite and application thereof
CN105532709A (en) * 2016-01-25 2016-05-04 北京市农林科学院 Pest killing and sterilization compound preparation containing sulfoxaflor and dimethomorph
CN112514910B (en) * 2019-09-17 2023-08-22 青岛奥迪斯生物科技有限公司 Insecticidal composition containing sulfoxaflor and bistrifluron

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050228027A1 (en) * 2004-04-08 2005-10-13 Yuanming Zhu Insecticidal N-substituted sulfoximines
US20070043086A1 (en) * 1998-06-17 2007-02-22 Christoph Erdelen Agents for controlling plant pests
WO2007095229A2 (en) * 2006-02-10 2007-08-23 Dow Agrosciences Llc Insecticidal n-substituted (6-haloalkylpyridin-3-yl)alkyl sulfoximines
WO2008104503A1 (en) * 2007-03-01 2008-09-04 Basf Se Pesticidal active mixtures comprising aminothiazoline compounds
WO2008125410A2 (en) * 2007-04-12 2008-10-23 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL78175A (en) * 1985-03-29 1989-10-31 Basf Ag Azolylmethyloxiranes,their preparation and their use as fungicide crop protection agents
DE19823396A1 (en) * 1998-05-26 1999-12-02 Bayer Ag Synergistic insecticidal mixtures
US20030224936A1 (en) * 1999-03-13 2003-12-04 Gerhard Kretzschmar Seed treatment composition
KR20080104187A (en) * 2006-03-10 2008-12-01 바스프 에스이 How to improve the plant's resistance to cold and / or frost
TWI381811B (en) * 2006-06-23 2013-01-11 Dow Agrosciences Llc A method to control insects resistant to common insecticides
TW200820902A (en) * 2006-11-08 2008-05-16 Dow Agrosciences Llc Use of N-substituted sulfoximines for control of invertebrate pests
AR066366A1 (en) * 2007-05-01 2009-08-12 Dow Agrosciences Llc PESTICIDED SYNERGIC BLENDS
CN102137593A (en) * 2008-08-28 2011-07-27 巴斯夫欧洲公司 Pesticidal mixtures comprising cyanosulfoximine compounds and spinetoram
WO2010040623A1 (en) * 2008-10-08 2010-04-15 Syngenta Participations Ag Pesticidal combinations containing sulfoxaflor

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070043086A1 (en) * 1998-06-17 2007-02-22 Christoph Erdelen Agents for controlling plant pests
US20050228027A1 (en) * 2004-04-08 2005-10-13 Yuanming Zhu Insecticidal N-substituted sulfoximines
WO2006060029A2 (en) * 2004-04-08 2006-06-08 Dow Agrosciences Llc Insecticidal n-substituted sulfoximines
WO2007095229A2 (en) * 2006-02-10 2007-08-23 Dow Agrosciences Llc Insecticidal n-substituted (6-haloalkylpyridin-3-yl)alkyl sulfoximines
WO2008104503A1 (en) * 2007-03-01 2008-09-04 Basf Se Pesticidal active mixtures comprising aminothiazoline compounds
WO2008125410A2 (en) * 2007-04-12 2008-10-23 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds

Cited By (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11930813B2 (en) 2007-04-12 2024-03-19 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds
US9888685B2 (en) 2007-04-12 2018-02-13 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds
US11033028B2 (en) 2007-04-12 2021-06-15 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds
US11930814B2 (en) 2007-04-12 2024-03-19 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds
WO2010023171A3 (en) * 2008-08-28 2010-12-23 Basf Se Pesticidal mixtures comprising cyanosulfoximine compounds and spinetoram
WO2010040623A1 (en) * 2008-10-08 2010-04-15 Syngenta Participations Ag Pesticidal combinations containing sulfoxaflor
CN102202511A (en) * 2008-10-08 2011-09-28 先正达参股股份有限公司 Pesticidal combinations containing sulfoxaflor
EP3120701A1 (en) * 2008-12-26 2017-01-25 Dow AgroSciences LLC Stable sulfoximine-insecticide compositions
AU2014256417B2 (en) * 2008-12-26 2016-04-14 Corteva Agriscience Llc Stable sulfoximine-insecticide compositions
US9125412B2 (en) 2008-12-26 2015-09-08 Dow Agrosciences Llc Stable insecticide compositions and methods for producing same
US8507532B2 (en) 2008-12-26 2013-08-13 Dow Agrosciences, Llc. Stable insecticide compositions and methods for producing same
AU2009330661B2 (en) * 2008-12-26 2014-09-11 Corteva Agriscience Llc Stable sulfoximine-insecticide compositions
JP2014167020A (en) * 2008-12-26 2014-09-11 Dow Agrosciences Llc Stable sulfoximine insecticide compositions
US8846717B2 (en) 2008-12-26 2014-09-30 Dow Agrosciences, Llc. Stable insecticide compositions and methods for producing same
WO2010074751A1 (en) * 2008-12-26 2010-07-01 Dow Agrosciences, Llc Stable sulfoximine-insecticide compositions
US9232798B2 (en) 2010-04-27 2016-01-12 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9232797B2 (en) 2010-04-27 2016-01-12 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9161539B2 (en) 2010-04-28 2015-10-20 Sumitomo Chemical Company, Limited Plant disease control composition and its use
KR101812361B1 (en) 2010-04-28 2017-12-26 스미또모 가가꾸 가부시키가이샤 Pesticidal composition and its use
US20130059894A1 (en) * 2010-04-28 2013-03-07 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9363998B2 (en) 2010-04-28 2016-06-14 Sumitomo Chemical Company, Limited Pesticidal composition and its use
US9375003B2 (en) 2010-04-28 2016-06-28 Sumitomo Chemical Company, Limited Plant disease control composition and its use
JP2011246459A (en) * 2010-04-28 2011-12-08 Sumitomo Chemical Co Ltd Pesticidal composition and use thereof
EP3146841A2 (en) 2010-06-30 2017-03-29 Bayer Intellectual Property GmbH Active agent combinations comprising penflufen and rynaxypyr or sulfoxaflor
US8598079B2 (en) 2010-06-30 2013-12-03 Bayer Cropscience Ag Active compound combinations
WO2012000946A2 (en) 2010-06-30 2012-01-05 Bayer Cropscience Ag Active ingredient combinations
AU2011314635B2 (en) * 2010-10-14 2015-08-13 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US9179671B2 (en) 2010-10-14 2015-11-10 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US20130190406A1 (en) * 2010-10-14 2013-07-25 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
WO2012050234A3 (en) * 2010-10-14 2012-09-20 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
JP2012102077A (en) * 2010-10-14 2012-05-31 Sumitomo Chemical Co Ltd Noxious organism-preventing/eliminating composition and noxious organism-preventing/eliminating method
EP2481284A3 (en) * 2011-01-27 2012-10-17 Basf Se Pesticidal mixtures

Also Published As

Publication number Publication date
BRPI0819823B1 (en) 2018-11-06
CN101909448A (en) 2010-12-08
EP2219456B1 (en) 2015-09-09
ES2554768T3 (en) 2015-12-23
BR122018016271B1 (en) 2022-06-14
BRPI0819823A2 (en) 2014-10-07
IL205622A0 (en) 2010-11-30
BR122018004457B1 (en) 2019-04-16
KR101605569B1 (en) 2016-03-22
US20110105321A1 (en) 2011-05-05
EP2219456A1 (en) 2010-08-25
US20140179518A1 (en) 2014-06-26
KR20100094994A (en) 2010-08-27
PL2219456T3 (en) 2016-03-31
JP2011503138A (en) 2011-01-27

Similar Documents

Publication Publication Date Title
JP5670328B2 (en) Pesticide mixture containing isoxazoline compound II
US20110105321A1 (en) Pesticidal Mixtures Comprising Cyanosulfoximine Compounds
EP3300602B1 (en) Pesticidal mixtures comprising a pyrazole compound
US20100029698A1 (en) Pesticidal Mixtures
KR20130132942A (en) Pesticidal active mixtures comprising pyrazole compounds
EP2320741A2 (en) Pesticidal mixtures comprising cyanosulfoximine compounds and spinetoram
JP2010503642A (en) Ternary pesticide mixture
WO2009007233A2 (en) Pesticidal mixtures comprising sulfonamides and one or more fungicides
AU2014202401A1 (en) Pesticidal mixtures
CA2857075A1 (en) Pesticidal mixtures

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880124587.X

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08851006

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 205622

Country of ref document: IL

WWE Wipo information: entry into national phase

Ref document number: 1688/KOLNP/2010

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2008851006

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2010533550

Country of ref document: JP

Ref document number: 12742766

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20107013146

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: PI0819823

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20100514